Product Name

  • Name

    4-Methoxyphenylacetyl chloride

  • EINECS -0
  • CAS No. 4693-91-8
  • Article Data119
  • CAS DataBase
  • Density 1.192 g/cm3
  • Solubility
  • Melting Point
  • Formula C9H9ClO2
  • Boiling Point 280.1 °C at 760 mmHg
  • Molecular Weight 184.622
  • Flash Point 100 °C
  • Transport Information UN 3265
  • Appearance colorless liquid
  • Safety 26-36/37/39-45
  • Risk Codes 14-34-37
  • Molecular Structure Molecular Structure of 4693-91-8 (4-Methoxyphenylacetyl chloride)
  • Hazard Symbols CorrosiveC
  • Synonyms Acetylchloride, (p-methoxyphenyl)- (6CI,7CI,8CI);(4-Methoxyphenyl)acetyl chloride;(p-Methoxyphenyl)acetyl chloride;2-(4-Methoxyphenyl)acetyl chloride;4-Methoxybenzeneacetyl chloride;p-Anisylacetyl chloride;p-Methoxyphenacetylchloride;
  • PSA 26.30000
  • LogP 2.00310

Synthetic route

4-Methoxyphenylacetic acid
104-01-8

4-Methoxyphenylacetic acid

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

Conditions
ConditionsYield
With thionyl chloride In toluene Heating;100%
With thionyl chloride In dichloromethane100%
With thionyl chloride; N,N-dimethyl-formamide In dichloromethane at 23℃;100%
p-Methoxybenzyl bromide
2746-25-0

p-Methoxybenzyl bromide

A

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

B

di-p-tolyl cadmium

di-p-tolyl cadmium

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: AcOH; aq. NaOH
2: thionyl chloride
View Scheme
p-methoxybenzylnitrile
104-47-2

p-methoxybenzylnitrile

A

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

B

di-p-tolyl cadmium

di-p-tolyl cadmium

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: AcOH; aq. NaOH
2: thionyl chloride
View Scheme
4-Methoxybenzyl alcohol
105-13-5

4-Methoxybenzyl alcohol

A

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

B

di-p-tolyl cadmium

di-p-tolyl cadmium

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: PBr3 / CH2Cl2
2: AcOH; aq. NaOH
3: thionyl chloride
View Scheme
1-methyl-pyrrolidin-2-one
872-50-4

1-methyl-pyrrolidin-2-one

4-Methoxyphenylacetic acid
104-01-8

4-Methoxyphenylacetic acid

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

Conditions
ConditionsYield
With thionyl chloride
4-hydroxyphenylacetate
156-38-7

4-hydroxyphenylacetate

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: sodium hydroxide / water / 12 h / 40 - 45 °C
2: thionyl chloride / 5 h / 60 °C
View Scheme
4-Methoxyphenylacetic acid
104-01-8

4-Methoxyphenylacetic acid

chloroacetyl chloride
79-04-9

chloroacetyl chloride

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

Conditions
ConditionsYield
In dichloromethane; N,N-dimethyl-formamide at 30℃; for 2h; Inert atmosphere;
N,O-dimethylhydroxylamine*hydrochloride
6638-79-5

N,O-dimethylhydroxylamine*hydrochloride

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-methoxy-2-(4-methoxyphenyl)-N-methylethanamide
267884-96-8

N-methoxy-2-(4-methoxyphenyl)-N-methylethanamide

Conditions
ConditionsYield
With pyridine In dichloromethane at 20℃; for 1h;100%
With pyridine In dichloromethane at 20℃; for 1h;88%
With pyridine; dmap; sodium hydrogencarbonate In diethyl ether
With pyridine In dichloromethane at 0℃; for 1h;
(S)-9-Trityloxy-nonan-4-ol
401788-86-1

(S)-9-Trityloxy-nonan-4-ol

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

(4-Methoxy-phenyl)-acetic acid (S)-1-propyl-6-trityloxy-hexyl ester

(4-Methoxy-phenyl)-acetic acid (S)-1-propyl-6-trityloxy-hexyl ester

Conditions
ConditionsYield
With potassium tert-butylate; tetra-(n-butyl)ammonium iodide In N,N-dimethyl-formamide100%
2-hydroxy-5-nitroaniline
99-57-0

2-hydroxy-5-nitroaniline

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-(2-hydroxy-5-nitro-phenyl)-2-(4-methoxy-phenyl)-acetamide

N-(2-hydroxy-5-nitro-phenyl)-2-(4-methoxy-phenyl)-acetamide

Conditions
ConditionsYield
With pyridine In tetrahydrofuran at 0 - 20℃; for 2h;100%
3-bromo-N-methylaniline
66584-32-5

3-bromo-N-methylaniline

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-(3-bromophenyl)-2-(4-methoxyphenyl)-N-methylacetamide
1268826-67-0

N-(3-bromophenyl)-2-(4-methoxyphenyl)-N-methylacetamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;100%
methoxybenzene
100-66-3

methoxybenzene

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

1,4-di(4-methoxyphenyl)ethanone
120-44-5

1,4-di(4-methoxyphenyl)ethanone

Conditions
ConditionsYield
With aluminum (III) chloride at 25℃; for 0.75h; Friedel-Crafts Acylation; Cooling;99%
With aluminum (III) chloride In dichloromethane at 20℃; for 1h; Friedel-Crafts Acylation;70%
With aluminium trichloride In 1,2-dichloro-ethane for 2h; Heating;67%
4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

O-methyl (p-methoxyphenyl)acetohydroxamate
112403-98-2

O-methyl (p-methoxyphenyl)acetohydroxamate

Conditions
ConditionsYield
99%
O-allylhydroxylamine hydrochloride
38945-21-0

O-allylhydroxylamine hydrochloride

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-(O-allylhydroxyl)-4-methoxyphenylacetamide
869089-90-7

N-(O-allylhydroxyl)-4-methoxyphenylacetamide

Conditions
ConditionsYield
With sodium carbonate In water; benzene at 0 - 20℃; for 12h;99%
1,3-dibromo-2-hydroxypropane
96-21-9

1,3-dibromo-2-hydroxypropane

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

2-bromo-1-(bromomethyl)ethyl 2-(4-methoxyphenyl)acetate

2-bromo-1-(bromomethyl)ethyl 2-(4-methoxyphenyl)acetate

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane Inert atmosphere;99%
N-methoxylamine hydrochloride
593-56-6

N-methoxylamine hydrochloride

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

O-methyl (p-methoxyphenyl)acetohydroxamate
112403-98-2

O-methyl (p-methoxyphenyl)acetohydroxamate

Conditions
ConditionsYield
With sodium carbonate In water; benzene for 5h; Ambient temperature;98%
With sodium carbonate In water; benzene at 23℃; for 12h; Inert atmosphere; Cooling with ice;67%
With potassium carbonate In water; ethyl acetate at 0 - 20℃;256.5 mg
3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-L-phenylalanine methyl ester
174905-91-0

3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-L-phenylalanine methyl ester

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-<(4-methoxyphenyl)acetyl>-3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-L-phenylalanine methyl ester
221332-90-7

N-<(4-methoxyphenyl)acetyl>-3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-L-phenylalanine methyl ester

Conditions
ConditionsYield
With sodium carbonate In benzene at 8 - 10℃; for 0.5h;98%
N-(4-cyanobenzyl)-6-aminopyrimidine-4-carboxamide hydrochloride

N-(4-cyanobenzyl)-6-aminopyrimidine-4-carboxamide hydrochloride

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

C22H19N5O3

C22H19N5O3

Conditions
ConditionsYield
With pyridine at 60℃; for 15h;98%
(+)404-3-(4-aminophenyl)-3-ethyl-2,6-piperidinedione
55511-44-9

(+)404-3-(4-aminophenyl)-3-ethyl-2,6-piperidinedione

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

C22H23FN2O4
1205648-10-7

C22H23FN2O4

Conditions
ConditionsYield
Stage #1: 4-methoxyphenyl-acetic chloride With bis-triphenylphosphine-palladium(II) chloride; O-benzoylquinidine; N-fluorobis(benzenesulfon)imide; N-ethyl-N,N-diisopropylamine In tetrahydrofuran at -78℃; for 8h; Inert atmosphere;
Stage #2: (+)404-3-(4-aminophenyl)-3-ethyl-2,6-piperidinedione With dmap In tetrahydrofuran at -78 - 20℃; Inert atmosphere; optical yield given as %de;
98%
N-methylhomoveratrylamine
3490-06-0

N-methylhomoveratrylamine

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-(3,4-dimethoxyphenethyl)-2-(4-methoxyphenyl)-N-methylacetamide

N-(3,4-dimethoxyphenethyl)-2-(4-methoxyphenyl)-N-methylacetamide

Conditions
ConditionsYield
With sodium hydroxide In chloroform; water98%
thiophenol
108-98-5

thiophenol

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

S-phenyl 2-(4-methoxyphenyl)ethanethioate
86211-05-4

S-phenyl 2-(4-methoxyphenyl)ethanethioate

Conditions
ConditionsYield
With triethylamine In toluene97%
4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

2-(4-Methoxyphenyl)ethanol
702-23-8

2-(4-Methoxyphenyl)ethanol

Conditions
ConditionsYield
With (1,3-dimethylimidazol-2-ylidene)borane In chloroform at 20℃; for 2h;97%
(1,3-dimethyl-1H-imidazol-3-ium-2-yl)bis(phenylthio)hydroborate

(1,3-dimethyl-1H-imidazol-3-ium-2-yl)bis(phenylthio)hydroborate

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

S-phenyl 2-(4-methoxyphenyl)ethanethioate
86211-05-4

S-phenyl 2-(4-methoxyphenyl)ethanethioate

Conditions
ConditionsYield
In chloroform at 20℃; for 2h;97%
salicylaldehyde
90-02-8

salicylaldehyde

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

3-(4-methoxyphenyl)coumarin
23000-33-1

3-(4-methoxyphenyl)coumarin

Conditions
ConditionsYield
With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate In benzene for 4h; Ambient temperature;96%
With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate In dichloromethane; water at 20℃;56%
3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-D-phenylalanine methyl ester
213692-58-1

3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-D-phenylalanine methyl ester

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-<(4-methoxxyphenyl)acetyl>-3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-D-phenylalanine methyl ester
213692-59-2

N-<(4-methoxxyphenyl)acetyl>-3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-D-phenylalanine methyl ester

Conditions
ConditionsYield
With sodium carbonate In water; benzene at 8 - 10℃; for 0.5h;96%
96%
1,2-benzenedithiole
17534-15-5

1,2-benzenedithiole

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

2-(4-Methoxy-benzylidene)-benzo[1,3]dithiole
62217-22-5

2-(4-Methoxy-benzylidene)-benzo[1,3]dithiole

Conditions
ConditionsYield
With tetrafluoroboric acid In diethyl ether at 105 - 110℃; for 0.166667h;95%
2-(4-bromophenyl)-N-methylethan-1-amine
725683-06-7

2-(4-bromophenyl)-N-methylethan-1-amine

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-(4-bromophenethyl)-2-(4-methoxyphenyl)-N-methylacetamide

N-(4-bromophenethyl)-2-(4-methoxyphenyl)-N-methylacetamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃;95%
2-(2-bromobenzyloxy)aniline
3434-04-6

2-(2-bromobenzyloxy)aniline

D-Prolin
344-25-2

D-Prolin

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

(R)-1-[(4-methoxyphenyl)acetyl]pyrrolidine-2-carboxylic acid

(R)-1-[(4-methoxyphenyl)acetyl]pyrrolidine-2-carboxylic acid

Conditions
ConditionsYield
With hydrogenchloride; sodium hydroxide In water; acetone95%
3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine
102226-41-5

3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

1-(2,3-dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-2-(4-methoxy-phenyl)-ethanone
1198154-13-0

1-(2,3-dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-2-(4-methoxy-phenyl)-ethanone

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 2h;95%
Propargylamine
2450-71-7

Propargylamine

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

2-(4-methoxyphenyl)-N-(prop-2-yn-1-yl)acetamide
1030779-93-1

2-(4-methoxyphenyl)-N-(prop-2-yn-1-yl)acetamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 3h; Huisgen Cycloaddition;95%
pyrrolidine
123-75-1

pyrrolidine

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

2-(4-methoxyphenyl)-1-(pyrrolidin-1-yl)ethan-1-one
123902-08-9

2-(4-methoxyphenyl)-1-(pyrrolidin-1-yl)ethan-1-one

Conditions
ConditionsYield
In dichloromethane at 20℃; for 5h; Inert atmosphere;95%
With triethylamine In dichloromethane at 20℃;4.18 g
1-amino-2-propene
107-11-9

1-amino-2-propene

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-allyl-2-(4-methoxyphenyl)acetamide

N-allyl-2-(4-methoxyphenyl)acetamide

Conditions
ConditionsYield
In dichloromethane for 4h; Cooling with ice;94%
(5-bromo-2-chloro-pyridin-3-ylmethyl)-methyl-amine
917473-39-3

(5-bromo-2-chloro-pyridin-3-ylmethyl)-methyl-amine

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-(5-bromo-2-chloro-pyridin-3-ylmethyl)-2-(4-methoxy-phenyl)-N-methyl-acetamide
917473-40-6

N-(5-bromo-2-chloro-pyridin-3-ylmethyl)-2-(4-methoxy-phenyl)-N-methyl-acetamide

Conditions
ConditionsYield
With 4-methyl-morpholine In dichloromethane at 0 - 23℃; for 18h;94%
With 4-methyl-morpholine In dichloromethane at 0 - 20℃; for 18.0667h;94%
2,5-dimethoxyaniline
102-56-7

2,5-dimethoxyaniline

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

N-(2,5-dimethoxyphenyl)-2-(4-methoxyphenyl)acetamide
256424-18-7

N-(2,5-dimethoxyphenyl)-2-(4-methoxyphenyl)acetamide

Conditions
ConditionsYield
In toluene at 20℃; for 1h;93%
In toluene; Petroleum ether1.83 g (93%)
recorcinol
108-46-3

recorcinol

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone
487-49-0

1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone

Conditions
ConditionsYield
With hydrogen fluoride at 20℃; for 12h; Product distribution / selectivity; Friedel-Crafts acylation; autoclave;92%
With aluminium trichloride; nitrobenzene
1,2,3-trimethoxybenzene
634-36-6

1,2,3-trimethoxybenzene

4-methoxyphenyl-acetic chloride
4693-91-8

4-methoxyphenyl-acetic chloride

1-(2-hydroxy-3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)ethanone
3606-32-4

1-(2-hydroxy-3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)ethanone

Conditions
ConditionsYield
With aluminium trichloride In carbon disulfide at 20℃;92%
With aluminium trichloride

4-Methoxyphenylacetyl chloride Specification

This chemical is called Benzenacetyl chloride, 4-methoxy-, and its systematic name is (4-methoxyphenyl)acetyl chloride. With the molecular formula of C9H9ClO2, its molecular weight is 184.62. The CAS registry number of this chemical is 4693-91-8. Additionally, its product categories are Aromatic Phenylacetic Acids and Derivatives; Acid Halides; Carbonyl Compounds; Organic Building Blocks. It should be stored at the temperature of 2-8°C.

Other characteristics of the Benzenacetyl chloride, 4-methoxy- can be summarised as followings: (1)ACD/LogP: 2.15; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.15; (4)ACD/LogD (pH 7.4): 2.15; (5)ACD/BCF (pH 5.5): 25.31; (6)ACD/BCF (pH 7.4): 25.31; (7)ACD/KOC (pH 5.5): 351.67; (8)ACD/KOC (pH 7.4): 351.67; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 26.3 Å2; (13)Index of Refraction: 1.524; (14)Molar Refractivity: 47.35 cm3; (15)Molar Volume: 154.7 cm3; (16)Polarizability: 18.77×10-24cm3; (17)Surface Tension: 37.9 dyne/cm; (18)Density: 1.192 g/cm3; (19)Flash Point: 100 °C; (20)Enthalpy of Vaporization: 51.88 kJ/mol; (21)Boiling Point: 280.1 °C at 760 mmHg; (22)Vapour Pressure: 0.00387 mmHg at 25°C. 

Production method of this chemical: The Benzenacetyl chloride, 4-methoxy- could be obtained by the reactant of (4-methoxy-phenyl)-acetic acid. This reaction needs the reagent of SOCl2, and the solvent of CH2Cl2. The other condition is heating.

Uses of this chemical: The Benzenacetyl chloride, 4-methoxy- could react with methoxybenzene, and obtain the 4,4'-dimethoxy-deoxybenzoin. This reaction needs the reagent of , and the solvent of AlCl3. The yield is 67 %. In addition, this reaction should be taken for 2 hours with the heating.

 

When you are using this chemical, please be cautious about it as the following: This chemical reacts violently with water and causes burns. It's irritating to respiratory system. Wear suitable protective clothing, gloves and eye/face protection if you use it. In case of contacting with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
1.SMILES: ClC(=O)Cc1ccc(OC)cc1
2.InChI: InChI=1/C9H9ClO2/c1-12-8-4-2-7(3-5-8)6-9(10)11/h2-5H,6H2,1H3
3.InChIKey: CXJOONIFSVSFAD-UHFFFAOYAG

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