Product Name

  • Name

    3'-METHOXYPHENACYL BROMIDE

  • EINECS 225-666-1
  • CAS No. 5000-65-7
  • Article Data92
  • CAS DataBase
  • Density 1.448 g/cm3
  • Solubility
  • Melting Point 60-62 °C(lit.)
  • Formula C9H9BrO2
  • Boiling Point 278.1 °C at 760 mmHg
  • Molecular Weight 229.073
  • Flash Point 122 °C
  • Transport Information UN 3261 8/PG 2
  • Appearance WHITE TO SLIGHTLY YELLOW-GREEN CRYST. POWDER
  • Safety 26-27-28-36/37/39-45
  • Risk Codes 34-36/37-22
  • Molecular Structure Molecular Structure of 5000-65-7 (3'-METHOXYPHENACYL BROMIDE)
  • Hazard Symbols CorrosiveC
  • Synonyms Acetophenone,2-bromo-3'-methoxy- (6CI,7CI,8CI);3-Methoxyphenacyl bromide;NSC 405833;m-(Bromoacetyl)anisole;m-Methoxyphenacyl bromide;a-Bromo-m-methoxyacetophenone;
  • PSA 26.30000
  • LogP 2.27280

Synthetic route

1-(3-Methoxyphenyl)ethanone
586-37-8

1-(3-Methoxyphenyl)ethanone

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

Conditions
ConditionsYield
With phenyltrimethylammonium tribromide In tetrahydrofuran at 20℃; for 1h;100%
With bromine In chloroform at 20℃; for 24h;100%
With bromine In chloroform at 20℃; for 4h;97%
acetophenone
98-86-2

acetophenone

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1.1: sulfuric acid; nitric acid / 0.33 h / -10 - -5 °C
2.1: hydrogenchloride; iron / water / Reflux
3.1: sulfuric acid / water / 0.5 h / 45 - 50 °C
3.2: 0.5 h / 0 - 5 °C
3.3: 2 h / 90 °C
4.1: 50 - 60 °C
5.1: N-Bromosuccinimide / ethyl acetate / 3 h / 20 °C
View Scheme
3-Nitroacetophenone
121-89-1

3-Nitroacetophenone

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1.1: hydrogenchloride; iron / water / Reflux
2.1: sulfuric acid / water / 0.5 h / 45 - 50 °C
2.2: 0.5 h / 0 - 5 °C
2.3: 2 h / 90 °C
3.1: 50 - 60 °C
4.1: N-Bromosuccinimide / ethyl acetate / 3 h / 20 °C
View Scheme
1-(3-aminophenyl)ethanone
99-03-6

1-(3-aminophenyl)ethanone

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: sulfuric acid / water / 0.5 h / 45 - 50 °C
1.2: 0.5 h / 0 - 5 °C
1.3: 2 h / 90 °C
2.1: 50 - 60 °C
3.1: N-Bromosuccinimide / ethyl acetate / 3 h / 20 °C
View Scheme
2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

benzenecarbothioamide
2227-79-4

benzenecarbothioamide

C16H13NOS
1013593-35-5

C16H13NOS

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 100℃; for 8h; Reflux;100%
1-[3-(2-pyridyl)-2-pyridyl]piperazine
1414942-27-0

1-[3-(2-pyridyl)-2-pyridyl]piperazine

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

1-(3-methoxyphenyl)-2-[4-[3-(2-pyridyl)-2-pyridyl]piperazin-1-yl]ethanone
1414942-20-3

1-(3-methoxyphenyl)-2-[4-[3-(2-pyridyl)-2-pyridyl]piperazin-1-yl]ethanone

Conditions
ConditionsYield
With potassium carbonate In acetonitrile Reflux;100%
With potassium carbonate In acetonitrile Reflux;100%
2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

potassium thioacetate
10387-40-3

potassium thioacetate

2-(acetylsulfanyl)-1-(3-methoxyphenyl)ethan-1-one
175657-38-2

2-(acetylsulfanyl)-1-(3-methoxyphenyl)ethan-1-one

Conditions
ConditionsYield
In ethanol; acetone at 20℃; for 2h;100%
phenylglyoxylic acid potassium salt
63468-90-6

phenylglyoxylic acid potassium salt

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

2-(3-methoxyphenyl)-2-oxoethyl 2-oxo-2-phenylacetate

2-(3-methoxyphenyl)-2-oxoethyl 2-oxo-2-phenylacetate

Conditions
ConditionsYield
In dimethyl sulfoxide at 20℃; for 0.5h; Inert atmosphere; Schlenk technique;100%
4-methoxypyridine
620-08-6

4-methoxypyridine

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

4-methoxy-1-(2-(3-methoxyphenyl)-2-oxoethyl)pyridin-1-ium bromide

4-methoxy-1-(2-(3-methoxyphenyl)-2-oxoethyl)pyridin-1-ium bromide

Conditions
ConditionsYield
In tetrahydrofuran for 0.5h; Reflux;99%
In acetonitrile at 45℃; Kinetics; pyridinolysis;
In acetone at 20℃; for 5h; Inert atmosphere;
[(2,2'-bipyridine)Cu(SeCF3)]2
1447204-38-7

[(2,2'-bipyridine)Cu(SeCF3)]2

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

C10H9F3O2Se

C10H9F3O2Se

Conditions
ConditionsYield
With potassium phosphate In dichloromethane at 45℃; for 16h; Inert atmosphere;98%
2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

1,2-bis-(diphenylphosphino)ethane
1663-45-2

1,2-bis-(diphenylphosphino)ethane

(3-methoxybenzoylmethyldiphenyl-2-diphenylphosphinoethylphosphonium)-bromide

(3-methoxybenzoylmethyldiphenyl-2-diphenylphosphinoethylphosphonium)-bromide

Conditions
ConditionsYield
In chloroform98%
In chloroform at 20℃; for 15h; Inert atmosphere; Schlenk technique;98%
p-toluidine
106-49-0

p-toluidine

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

1-(3-methoxyphenyl)-2-(4-methylphenylamino)ethanone

1-(3-methoxyphenyl)-2-(4-methylphenylamino)ethanone

Conditions
ConditionsYield
With sodium hydrogencarbonate In ethanol; water at 20℃; for 24h;98%
2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

2-bromo-1-(3-methoxyphenyl)ethan-1-one oxime

2-bromo-1-(3-methoxyphenyl)ethan-1-one oxime

Conditions
ConditionsYield
With hydroxylamine hydrochloride In methanol; water at 0 - 20℃;98%
2-Amino-4-methylpyridine
695-34-1

2-Amino-4-methylpyridine

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

2-(3-Methoxy-phenyl)-7-methyl-imidazo[1,2-a]pyridine

2-(3-Methoxy-phenyl)-7-methyl-imidazo[1,2-a]pyridine

Conditions
ConditionsYield
In neat (no solvent) at 25 - 30℃; Milling; Green chemistry;98%
2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

hex-1-yne
693-02-7

hex-1-yne

2-(4-butyl-1H-1,2,3-triazol-1-yl)-1-(3-methoxyphenyl)ethanone
1536405-99-8

2-(4-butyl-1H-1,2,3-triazol-1-yl)-1-(3-methoxyphenyl)ethanone

Conditions
ConditionsYield
With sodium azide; sodium ascorbate In ethanol; water at 20℃; for 0.333333h; regioselective reaction;97%
With sodium azide; sodium L-ascorbate In ethanol; water at 85℃; for 0.416667h;96%
2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

7-hydroxy-4-(4-methoxyphenyl)-8-methyl-2H-2-chromenone
370583-62-3

7-hydroxy-4-(4-methoxyphenyl)-8-methyl-2H-2-chromenone

4-(4-methoxyphenyl)-7-[2-(3-methoxyphenyl)-2-oxoethoxy]-8-methyl-2-chromenone
500203-99-6

4-(4-methoxyphenyl)-7-[2-(3-methoxyphenyl)-2-oxoethoxy]-8-methyl-2-chromenone

Conditions
ConditionsYield
With potassium carbonate In acetone at 50 - 56℃; Williamson reaction;96%
N-Cbz-L-Phe
1161-13-3

N-Cbz-L-Phe

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

2-(1-(S)-((Phenylmethoxy)carbonyl)-amino-2-phenylethyl)-4-(4-methoxyphenyl)-imidazole

2-(1-(S)-((Phenylmethoxy)carbonyl)-amino-2-phenylethyl)-4-(4-methoxyphenyl)-imidazole

Conditions
ConditionsYield
With ammonium acetate; caesium carbonate In water; N,N-dimethyl-formamide96%
4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

thiosemicarbazide
79-19-6

thiosemicarbazide

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

(E)-2-(2-(4-methoxybenzylidene)hydrazinyl)-4-(3-methoxyphenyl)thiazole

(E)-2-(2-(4-methoxybenzylidene)hydrazinyl)-4-(3-methoxyphenyl)thiazole

Conditions
ConditionsYield
In water at 25 - 30℃;96%
3-Hydroxy-4-methyl-7,8,9,10-tetrahydro-6H-dibenzopyran-6-one
55047-37-5

3-Hydroxy-4-methyl-7,8,9,10-tetrahydro-6H-dibenzopyran-6-one

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

3-[2-(3-methoxyphenyl)-2-oxoethoxy]-4-methyl-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one

3-[2-(3-methoxyphenyl)-2-oxoethoxy]-4-methyl-7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one

Conditions
ConditionsYield
Stage #1: 3-Hydroxy-4-methyl-7,8,9,10-tetrahydro-6H-dibenzopyran-6-one With potassium carbonate In acetone at 50 - 56℃; Williamson reaction;
Stage #2: 2-bromo-3'-methoxyacetophenone In acetone for 1h; Williamson reaction; Heating;
95%
2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

diethyl 1H-pyrazole-3,5-dicarboxylate
37687-24-4

diethyl 1H-pyrazole-3,5-dicarboxylate

C18H20N2O6
1316761-36-0

C18H20N2O6

Conditions
ConditionsYield
With potassium carbonate In acetone at 20℃; for 12h;95%
benzophenone hydrazone
5350-57-2

benzophenone hydrazone

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

p-nitrophenyl isothiocyanate
2131-61-5

p-nitrophenyl isothiocyanate

N-(diphenylmethylene)-4-(3-methoxyphenyl)-2-(4-nitrophenylimino)thiazol-3(2H)-amine

N-(diphenylmethylene)-4-(3-methoxyphenyl)-2-(4-nitrophenylimino)thiazol-3(2H)-amine

Conditions
ConditionsYield
With triethylamine In ethanol for 3h; Reflux;95%
thiosemicarbazide
79-19-6

thiosemicarbazide

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

2,4-Dimethoxybenzaldehyde
613-45-6

2,4-Dimethoxybenzaldehyde

(E)-2-(2-(2,4-dimethoxybenzylidene)hydrazinyl)-4-(3-methoxyphenyl)thiazole

(E)-2-(2-(2,4-dimethoxybenzylidene)hydrazinyl)-4-(3-methoxyphenyl)thiazole

Conditions
ConditionsYield
In water at 25 - 30℃;95%
isonicotinic acid ethylester
1570-45-2

isonicotinic acid ethylester

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

4-(ethoxycarbonyl)-1-[2-(3-methoxyphenyl)-2-oxoethyl]pyridinium bromide

4-(ethoxycarbonyl)-1-[2-(3-methoxyphenyl)-2-oxoethyl]pyridinium bromide

Conditions
ConditionsYield
In acetone at 20℃; for 24h;95%
5-hydroxy-2,2-dimethyl-2H-chromene-6-carbaldehyde
54287-99-9

5-hydroxy-2,2-dimethyl-2H-chromene-6-carbaldehyde

2-bromo-3'-methoxyacetophenone
5000-65-7

2-bromo-3'-methoxyacetophenone

(7,7-dimethyl-7H-furo[2,3-f]chromen-2-yl)(3-methoxyphenyl)methanone

(7,7-dimethyl-7H-furo[2,3-f]chromen-2-yl)(3-methoxyphenyl)methanone

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 20 - 120℃; for 4h;95%

2-Bromo-3'-methoxyacetophenone Specification

The 2-Bromo-3'-methoxyacetophenone is an organic compound with the formula C9H9BrO2. The IUPAC name of this chemical is 2-bromo-1-(3-methoxyphenyl)ethanone. With the CAS registry number 5000-65-7, it is also named as Ethanone, 2-bromo-1-(3-methoxyphenyl)-. The product's categories are Aromatic Halides (substituted); Analytical Chemistry; Carboxyl Group Labeling Reagents for HPLC; HPLC Labeling Reagents; UV Detection (HPLC Labeling Reagents). Besides, it is a white to slightly yellow-green cryst, which should be stored in a cool,dry place at temperature of 0 - 6 °C.

Physical properties about 2-Bromo-3'-methoxyacetophenone are: (1)ACD/LogP: 2.37; (2)ACD/LogD (pH 5.5): 2.37; (3)ACD/LogD (pH 7.4): 2.37; (4)ACD/BCF (pH 5.5): 36.97; (5)ACD/BCF (pH 7.4): 36.97; (6)ACD/KOC (pH 5.5): 461.17; (7)ACD/KOC (pH 7.4): 461.17; (8)#H bond acceptors: 2; (9)#Freely Rotating Bonds: 3; (10)Polar Surface Area: 26.3 Å2; (11)Index of Refraction: 1.554; (12)Molar Refractivity: 50.69 cm3; (13)Molar Volume: 158.1 cm3; (14)Polarizability: 20.09×10-24cm3; (15)Surface Tension: 41.4 dyne/cm; (16)Density: 1.448 g/cm3; (17)Flash Point: 122 °C; (18)Enthalpy of Vaporization: 51.67 kJ/mol; (19)Boiling Point: 278.1 °C at 760 mmHg; (20)Vapour Pressure: 0.00434 mmHg at 25°C.

Preparation: this chemical can be prepared by 1-(3-methoxy-phenyl)-ethanone. This reaction will need reagentBr2, HCl and solvent acetic acid. The reaction temperature is 20 °C.



Uses of 2-Bromo-3'-methoxyacetophenone: it can be used to produce 2-(3-methoxy-phenyl)-imidazo[1,2-a]pyrimidine by heating. It will need solvent 1,2-dimethoxy-ethane with reaction time of 48 hours. The yield is about 75%.

When you are using this chemical, please be cautious about it as the following:
It is harmful if swallowed and can cause burns. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. Besides, this chemical is irritating to eyes and respiratory system. After contact with skin, take off immediately all contaminated clothing, and wash immediately with plenty of ... (to be specified by the manufacturer). When you are using it, wear suitable gloves and eye/face protection. In case of accident or if you feel unwell seek medical advice immediately (show the label where possible).

You can still convert the following datas into molecular structure:
(1)SMILES: BrCC(=O)c1cc(OC)ccc1
(2)InChI: InChI=1/C9H9BrO2/c1-12-8-4-2-3-7(5-8)9(11)6-10/h2-5H,6H2,1H3
(3)InChIKey: IOOHBIFQNQQUFI-UHFFFAOYAC
(4)Std. InChI: InChI=1S/C9H9BrO2/c1-12-8-4-2-3-7(5-8)9(11)6-10/h2-5H,6H2,1H3
(5)Std. InChIKey: IOOHBIFQNQQUFI-UHFFFAOYSA-N

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