Conditions | Yield |
---|---|
With thionyl chloride In toluene Heating; | 100% |
With thionyl chloride In dichloromethane | 100% |
With thionyl chloride; N,N-dimethyl-formamide In dichloromethane at 23℃; | 100% |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: AcOH; aq. NaOH 2: thionyl chloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: AcOH; aq. NaOH 2: thionyl chloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: PBr3 / CH2Cl2 2: AcOH; aq. NaOH 3: thionyl chloride View Scheme |
1-methyl-pyrrolidin-2-one
4-Methoxyphenylacetic acid
4-methoxyphenyl-acetic chloride
Conditions | Yield |
---|---|
With thionyl chloride |
Conditions | Yield |
---|---|
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
chloroacetyl chloride
4-methoxyphenyl-acetic chloride
Conditions | Yield |
---|---|
In dichloromethane; N,N-dimethyl-formamide at 30℃; for 2h; Inert atmosphere; |
N,O-dimethylhydroxylamine*hydrochloride
4-methoxyphenyl-acetic chloride
N-methoxy-2-(4-methoxyphenyl)-N-methylethanamide
Conditions | Yield |
---|---|
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
4-methoxyphenyl-acetic chloride
Conditions | Yield |
---|---|
With potassium tert-butylate; tetra-(n-butyl)ammonium iodide In N,N-dimethyl-formamide | 100% |
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 0 - 20℃; for 2h; | 100% |
3-bromo-N-methylaniline
4-methoxyphenyl-acetic chloride
N-(3-bromophenyl)-2-(4-methoxyphenyl)-N-methylacetamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
methoxybenzene
4-methoxyphenyl-acetic chloride
1,4-di(4-methoxyphenyl)ethanone
Conditions | Yield |
---|---|
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
O-methyl (p-methoxyphenyl)acetohydroxamate
Conditions | Yield |
---|---|
99% |
O-allylhydroxylamine hydrochloride
4-methoxyphenyl-acetic chloride
N-(O-allylhydroxyl)-4-methoxyphenylacetamide
Conditions | Yield |
---|---|
With sodium carbonate In water; benzene at 0 - 20℃; for 12h; | 99% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane Inert atmosphere; | 99% |
N-methoxylamine hydrochloride
4-methoxyphenyl-acetic chloride
O-methyl (p-methoxyphenyl)acetohydroxamate
Conditions | Yield |
---|---|
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
4-methoxyphenyl-acetic chloride
N-<(4-methoxyphenyl)acetyl>-3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-L-phenylalanine methyl ester
Conditions | Yield |
---|---|
With sodium carbonate In benzene at 8 - 10℃; for 0.5h; | 98% |
4-methoxyphenyl-acetic chloride
Conditions | Yield |
---|---|
With pyridine at 60℃; for 15h; | 98% |
(+)404-3-(4-aminophenyl)-3-ethyl-2,6-piperidinedione
4-methoxyphenyl-acetic chloride
C22H23FN2O4
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With sodium hydroxide In chloroform; water | 98% |
thiophenol
4-methoxyphenyl-acetic chloride
S-phenyl 2-(4-methoxyphenyl)ethanethioate
Conditions | Yield |
---|---|
With triethylamine In toluene | 97% |
Conditions | Yield |
---|---|
With (1,3-dimethylimidazol-2-ylidene)borane In chloroform at 20℃; for 2h; | 97% |
4-methoxyphenyl-acetic chloride
S-phenyl 2-(4-methoxyphenyl)ethanethioate
Conditions | Yield |
---|---|
In chloroform at 20℃; for 2h; | 97% |
salicylaldehyde
4-methoxyphenyl-acetic chloride
3-(4-methoxyphenyl)coumarin
Conditions | Yield |
---|---|
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
4-methoxyphenyl-acetic chloride
N-<(4-methoxxyphenyl)acetyl>-3,5-dimethoxy-2-<<(4-methoxyphenyl)methyl>thio>-D-phenylalanine methyl ester
Conditions | Yield |
---|---|
With sodium carbonate In water; benzene at 8 - 10℃; for 0.5h; | 96% |
96% |
1,2-benzenedithiole
4-methoxyphenyl-acetic chloride
2-(4-Methoxy-benzylidene)-benzo[1,3]dithiole
Conditions | Yield |
---|---|
With tetrafluoroboric acid In diethyl ether at 105 - 110℃; for 0.166667h; | 95% |
2-(4-bromophenyl)-N-methylethan-1-amine
4-methoxyphenyl-acetic chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; | 95% |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium hydroxide In water; acetone | 95% |
3,4-dihydro-2H-pyrido[4,3-b][1,4]oxazine
4-methoxyphenyl-acetic chloride
1-(2,3-dihydro-pyrido[4,3-b][1,4]oxazin-4-yl)-2-(4-methoxy-phenyl)-ethanone
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 2h; | 95% |
Propargylamine
4-methoxyphenyl-acetic chloride
2-(4-methoxyphenyl)-N-(prop-2-yn-1-yl)acetamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 3h; Huisgen Cycloaddition; | 95% |
pyrrolidine
4-methoxyphenyl-acetic chloride
2-(4-methoxyphenyl)-1-(pyrrolidin-1-yl)ethan-1-one
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 5h; Inert atmosphere; | 95% |
With triethylamine In dichloromethane at 20℃; | 4.18 g |
Conditions | Yield |
---|---|
In dichloromethane for 4h; Cooling with ice; | 94% |
(5-bromo-2-chloro-pyridin-3-ylmethyl)-methyl-amine
4-methoxyphenyl-acetic chloride
N-(5-bromo-2-chloro-pyridin-3-ylmethyl)-2-(4-methoxy-phenyl)-N-methyl-acetamide
Conditions | Yield |
---|---|
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
4-methoxyphenyl-acetic chloride
N-(2,5-dimethoxyphenyl)-2-(4-methoxyphenyl)acetamide
Conditions | Yield |
---|---|
In toluene at 20℃; for 1h; | 93% |
In toluene; Petroleum ether | 1.83 g (93%) |
recorcinol
4-methoxyphenyl-acetic chloride
1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone
Conditions | Yield |
---|---|
With hydrogen fluoride at 20℃; for 12h; Product distribution / selectivity; Friedel-Crafts acylation; autoclave; | 92% |
With aluminium trichloride; nitrobenzene |
1,2,3-trimethoxybenzene
4-methoxyphenyl-acetic chloride
1-(2-hydroxy-3,4-dimethoxyphenyl)-2-(4-methoxyphenyl)ethanone
Conditions | Yield |
---|---|
With aluminium trichloride In carbon disulfide at 20℃; | 92% |
With aluminium trichloride |
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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