CAS No.3233-32-7,4-hydroxyphenyl acetate Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

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4-Hydroxyphenyl acetate

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1,4-Benzenediol,1-acetate

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Baoji Guokang Healthchem co.,ltd

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4-Acetoxyphenol

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Hangzhou Fandachem Co.,Ltd

4-Hydroxyphenyl acetate cas 3233-32-7Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

4-Hydroxyphenyl acetate cas 3233-32-7

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4-hydroxyphenyl acetate

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Pure Chemistry Scientific Inc.

1,4-Benzenediol,1-acetate Application:80071382

1,4-Benzenediol,1-acetate

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GZ HONESTCHEM CO., LTD

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4-Acetoxyphenol

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Sparrow Chemical Co.,Ltd

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Shanghai Haoyuan Chemexpress Co., Ltd.

4-Hydroxyphenyl acetate

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qingcang（shanghai） Medical Technology Co., Ltd.

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Synthetic route

: 1205-91-0
benzene-1,4-diyl diacetate

: 123-31-9
hydroquinone

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With potassium carbonate In dimethyl sulfoxide at 25℃; Green chemistry; regioselective reaction;	99%

: 177490-82-3
(4-acetoxyphenyl)boronic acid

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With menadione; sodium hydrogencarbonate; sodium L-ascorbate In ethanol; water at 20℃; under 760.051 Torr; for 24h; pH=8.5; Darkness; Green chemistry;	98%
With oxygen; N-ethyl-N,N-diisopropylamine; [5,6]fullerene-C70 In chloroform; toluene at 20℃; for 12h; Irradiation;	98%

: 64-19-7
acetic acid

: 123-31-9
hydroquinone

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With 50wtpercent Cs2.5H0.5PW12O40 supported on MCM-41 In acetonitrile at 50℃; for 0.5h;	97%

: 4-[(t-butyldimethylsilyl)oxy]phenyl acetate

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With potassium hydrogen difluoride In methanol at 20℃; for 1h;	97%

: 108-24-7
acetic anhydride

: 123-31-9
hydroquinone

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With silica-sulfuric acid nanoparticles In neat (no solvent) at 20℃; for 0.166667h;	95%
With acetic acid at 110℃; for 2h;	94%
With acetic acid at 110℃; Inert atmosphere;	86%

: 225529-40-8
4-benzoyloxy phenyl acetate

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With phosphate buffer; Lipase PS-C In tetrahydrofuran for 4h; Ambient temperature; pH=7;	93%

: acetic acid 4-methoxymethoxy-phenyl ester

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
sodium hydrogen sulfate; silica gel In dichloromethane at 20℃; for 1.5h;	91%

: 82969-01-5
4-acetoxyphenyl tosylate

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With cerium(III) chloride; sodium iodide In acetonitrile for 4h; tosylate cleavage; Heating;	90%

: 108-24-7
acetic anhydride

: 123-31-9
hydroquinone

A: 1205-91-0
benzene-1,4-diyl diacetate

B: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With pyridine hydrogenfluoride In dichloromethane at 20℃; for 1.5h;	A 13% B 74%
With pyridine for 1h;
With sodium carbonate anfangs unter Kuehlung;

...Expand

: 53135-65-2
4-(prop-2-yn-1-yloxy)phenyl acetate

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In benzene at 100℃; for 24h; Product distribution; Further Variations:; Solvents; Temperatures; reaction times;	61%

: 122-79-2
Phenyl acetate

A: 102-29-4
Resorcinol monoacetate

B: 2848-25-1
2-acetoxyphenol

C: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With dihydrogen peroxide at -40℃; for 0.5h; Product distribution; HF - SbF5;	A 56% B 5% C 26%

...Expand

: 75-36-5
acetyl chloride

: 123-31-9
hydroquinone

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran for 2h;	52%
With hydrogenchloride In water at 50 - 110℃; for 3h;

: 6311-66-6
4-(benzyloxy)phenyl acetate

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In ethanol at 52℃; under 2585.7 Torr; for 3h;	45.3%
In toluene
With hydrogen; 10% Pd/C (containing 50% water) In tetrahydrofuran; ethanol at 20℃; under 1140.08 Torr; for 2h;

: 4-oxo-1-(5-oxo-3-((triisopropylsilyl)oxy)pentyl)cyclohexa-2,5-dien-1-yl acetate

A: 3233-32-7
hydroquinone monoacetate

B: (1R,2R,4aR,8aS)-1-formyl-7-oxo-2-((triisopropylsilyl)oxy)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-4a-yl acetate

Conditions

Conditions	Yield
With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine In dichloromethane at 0℃; for 12h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Michael Addition;	A 35% B 40%

: 65109-75-3
N-(phenoxy)-4-methylbenzenesulfonamide

: 64-19-7
acetic acid

A: 2848-25-1
2-acetoxyphenol

B: 3233-32-7
hydroquinone monoacetate

C: 65109-81-1
2-hydroxyphenyl p-toluenesulfonimidate

D: 65109-80-0
4-hydroxyphenyl trifluoromethanesulfonate

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid for 18h; Ambient temperature;	A n/a B 11% C 23% D 16%

...Expand

: 122-79-2
Phenyl acetate

A: 102-29-4
Resorcinol monoacetate

B: 2848-25-1
2-acetoxyphenol

C: 3233-32-7
hydroquinone monoacetate

D: 108-95-2
phenol

Conditions

Conditions	Yield
With dihydrogen peroxide at -60℃; for 0.5h; Product distribution; HF - BF3; relative proportion;	A n/a B n/a C n/a D 22%

...Expand

: 4-oxo-1-(5-oxo-3-((triisopropylsilyl)oxy)pentyl)cyclohexa-2,5-dien-1-yl acetate

A: 3233-32-7
hydroquinone monoacetate

B: 1-formyl-7-oxo-2-((triisopropylsilyl)oxy)-1,2,3,4,4a,7,8,8a-octahydronaphthalen-4a-yl acetate

Conditions

Conditions	Yield
With L-proline In dichloromethane at 25℃; for 10h; Michael Addition;	A n/a B 20%

: 408339-53-7
carbonic acid-(4-acetoxy-phenyl ester)-benzyl ester

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With ethanol; platinum Hydrogenolyse;

: 79-21-0
peracetic acid

: 108-24-7
acetic anhydride

: 123-08-0
4-hydroxy-benzaldehyde

: 104-15-4
toluene-4-sulfonic acid

A: 1205-91-0
benzene-1,4-diyl diacetate

B: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
unter Kuehlung;

...Expand

: 79-21-0
peracetic acid

: 123-08-0
4-hydroxy-benzaldehyde

A: 1205-91-0
benzene-1,4-diyl diacetate

B: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With acetic anhydride; toluene-4-sulfonic acid

...Expand

: 75-36-5
acetyl chloride

: 123-31-9
hydroquinone

A: 1205-91-0
benzene-1,4-diyl diacetate

B: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With pyridine unter starker Kuehlung;
With ethanol; sodium ethanolate

...Expand

: 79-21-0
peracetic acid

: 99-93-4
4-Hydroxyacetophenone

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
With sodium hydroxide In water for 0.25h; Ambient temperature;

: 99-93-4
4-Hydroxyacetophenone

A: 3233-32-7
hydroquinone monoacetate

B: 123-31-9
hydroquinone

Conditions

Conditions	Yield
With 4-hydroxyacetophenone monooxygenase from P. fluorescens ACB; oxygen; NADPH In phosphate buffer at 30℃; for 1h; pH=8.0; Enzyme kinetics; Baeyer-Villiger oxidation;
With 4-hydroxyacetophenone monooxygenase from Pseudomonas fluorescens; phosphite dehydrogenase; NADPH In dimethyl sulfoxide at 24℃; Tris/HCl buffer; Enzymatic reaction;

: 103-16-2
4-Benzyloxyphenol

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 53 percent / Et3N / CH2Cl2 / 1 h / Ambient temperature 2: 45.3 percent / H2 / 5 percent Pd/C (Strem) / ethanol / 3 h / 52 °C / 2585.7 Torr View Scheme

: 74206-92-1
carbonic acid benzyl ester-(4-hydroxy-phenyl ester)

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: pyridine / 20 °C 2: ethanol; platinum / Hydrogenolyse View Scheme

: 123-31-9
hydroquinone

: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: water 2: pyridine / 20 °C 3: ethanol; platinum / Hydrogenolyse View Scheme
Multi-step reaction with 3 steps 1.1: 1H-imidazole / N,N-dimethyl-formamide / 0.17 h / 20 °C / Inert atmosphere 1.2: 2 h / 20 °C / Inert atmosphere 2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.08 h 2.2: 20 °C / Inert atmosphere 3.1: potassium hydrogen difluoride / methanol / 1 h / 20 °C View Scheme

: 959957-51-8
4-acetoxy-4-isopropyl-2,5-cyclohexadienone

A: 3233-32-7
hydroquinone monoacetate

B: 123-31-9
hydroquinone

C: 106-51-4
p-benzoquinone

D: 4-hydroxy-4-isopropylcyclohexa-2,5-dien-1-one

Conditions

Conditions	Yield
With perchloric acid In water; acetonitrile at 80℃; pH=1.0; Kinetics; Product distribution; Further Variations:; pH-values; Reagents;

...Expand

: 4-acetoxy-4-tert-butyl-2,5-cyclohexadienone

A: 3240-34-4
[bis(acetoxy)iodo]benzene

B: 3233-32-7
hydroquinone monoacetate

C: 123-31-9
hydroquinone

D: 106-51-4
p-benzoquinone

Conditions

Conditions	Yield
With perchloric acid In water; acetonitrile at 30℃; pH=1.0; Kinetics; Further Variations:; pH-values; Reagents; Temperatures;

...Expand

: 64-19-7
acetic acid

: 108-95-2
phenol

: 4-acetoxy-5-bromocyclohex-2-enone

B: 3233-32-7
hydroquinone monoacetate

Conditions

Conditions	Yield
Multistep reaction. Title compound not separated from byproducts.;

...Expand

: 930608-31-4
2,2,2-trichloro-acetimidic acid 4-(tert-butyl-dimethyl-silanyloxy)-but-2-enyl ester

: 3233-32-7
hydroquinone monoacetate

: (S)-2-(4-acetoxyphenoxy)but-3-enyloxy(tert-butyl)dimethylsilane

Conditions

Conditions	Yield
With [(S)-COP-OAc]2 In dichloromethane at 38℃; for 36h;	97%

: 3233-32-7
hydroquinone monoacetate

: 2524-04-1
diethyl phosphorochloridothioate

: Acetic acid 4-(diethoxy-thiophosphoryloxy)-phenyl ester

Conditions

Conditions	Yield
With PEG-400; aluminum oxide; sodium hydroxide; water 1.) MeOH, r.t., 30 min, 2.) r.t., 1 h;	95%

: 3233-32-7
hydroquinone monoacetate

: 18162-48-6
tert-butyldimethylsilyl chloride

: 4-[(t-butyldimethylsilyl)oxy]phenyl acetate

Conditions

Conditions	Yield
With 1H-imidazole; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 20℃; for 2h;	93%

: 930608-34-7
acetic acid 5-trichloroacetimidoyloxy-pent-3-enyl ester

: 3233-32-7
hydroquinone monoacetate

: (R)-3-(4-acetoxyphenoxy)pent-4-enyl acetate

Conditions

Conditions	Yield
With [(S)-COP-OAc]2 In dichloromethane at 38℃; for 48h;	93%

: 24424-99-5
di-tert-butyl dicarbonate

: 3233-32-7
hydroquinone monoacetate

: 1072798-28-7
4-(tert-butoxycarbonyloxy)acetoxybenzene

Conditions

Conditions	Yield
With carbon tetrabromide at 35 - 40℃; for 10h; Neat (no solvent); chemoselective reaction;	92%

: 110-87-2
3,4-dihydro-2H-pyran

: 3233-32-7
hydroquinone monoacetate

: 134142-87-3
2-(4-Acetoxyphenoxy)tetrahydropyran

Conditions

Conditions	Yield
	91%

: 3233-32-7
hydroquinone monoacetate

: 56777-24-3
benzyl (S)-Lactate

: C18H18O5

Conditions

Conditions	Yield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0 - 20℃; for 5h;	90%

: 30365-54-9
ethyl (S)-2-bromopropionate

: 3233-32-7
hydroquinone monoacetate

: C13H16O5

Conditions

Conditions	Yield
With sodium hydroxide In water Product distribution / selectivity;	88%

: 1572-71-0
(E)-2-methylpenta-2,4-dien-1-ol

: 3233-32-7
hydroquinone monoacetate

: 277332-46-4
Acetic acid 4-((E)-2-methyl-penta-2,4-dienyloxy)-phenyl ester

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran Etherification; Mitsunobu reaction;	87%

: 17102-64-6
Sorbyl alcohol

: 3233-32-7
hydroquinone monoacetate

: 277332-44-2
Acetic acid 4-[((2E,4E)-hexa-2,4-dienyl)oxy]-phenyl ester

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran Etherification; Mitsunobu reaction;	86%

: 3233-32-7
hydroquinone monoacetate

: 814-68-6
acryloyl chloride

: p-acetoxyphenyl acrylate

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran for 2h;	85%

: 75-44-5
phosgene

: 3233-32-7
hydroquinone monoacetate

: (2'R,P)-1,12-bis-(2'-hydroxypropyl)-2,4,6,7,9,11-hexamethoxy-3,10-perylenequinone

: (2'R,P)-1,12-bis-(2'-(4''-acetoxy)phenoxycarbonyloxypropyl)-2,4,6,7,9,11-hexamethoxy-3,10-perylenequinone

Conditions

Conditions	Yield
Stage #1: phosgene; (2'R,P)-1,12-bis-(2'-hydroxypropyl)-2,4,6,7,9,11-hexamethoxy-3,10-perylenequinone With triethylamine In tetrahydrofuran; toluene; acetonitrile at 0℃; for 0.333333h; Stage #2: hydroquinone monoacetate With dmap; triethylamine In tetrahydrofuran at 20℃; for 16h; Further stages.;	85%

...Expand

: 687-47-8
(S)-Ethyl lactate

: 3233-32-7
hydroquinone monoacetate

: C13H16O5

Conditions

Conditions	Yield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0 - 20℃; for 5h;	85%

: 3233-32-7
hydroquinone monoacetate

: 67065-89-8
(2E)-4-methyl-2,4-pentadien-1-ol

: 277332-45-3
Acetic acid 4-((E)-4-methyl-penta-2,4-dienyloxy)-phenyl ester

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran Etherification; Mitsunobu reaction;	84%

: 358-23-6
trifluoromethylsulfonic anhydride

: 3233-32-7
hydroquinone monoacetate

: 4-(((trifluoromethyl)sulfonyl)oxy)phenyl acetate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at -78 - 0℃;	83%

: 4949-20-6
(E)-2,4-pentadien-1-ol

: 3233-32-7
hydroquinone monoacetate

: 277332-43-1
Acetic acid 4-[((E)-penta-2,4-dienyl)oxy]-phenyl ester

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran Etherification; Mitsunobu reaction;	82%

: 27871-49-4
(S)-Methyl lactate

: 3233-32-7
hydroquinone monoacetate

A: 111842-06-9
methyl (R)-2-(4-acetoxyphenoxy)propionate

B: C12H14O5

Conditions

Conditions	Yield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0 - 20℃; for 5h;	A 82% B n/a

...Expand

: 3233-32-7
hydroquinone monoacetate

: 108-88-3
toluene

: 6311-66-6
4-(benzyloxy)phenyl acetate

Conditions

Conditions	Yield
With di-tert-butyl peroxide; 1,3-di-tert-butylimidazolium at 130℃; for 24h; Green chemistry;	82%
With di-tert-butyl peroxide; 1,3-di-tert-butylimidazolium at 130℃; for 24h;	82%

: 25236-64-0
2,2,2-trifluoroethyl methanesulfonate

: 3233-32-7
hydroquinone monoacetate

: 76579-45-8
4-((trifluoro)ethoxy)phenyl acetate

Conditions

Conditions	Yield
With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide at 140℃; for 20h;	80%

: 1111-97-3
3-chloro-3-methylbut-1-yne

: 3233-32-7
hydroquinone monoacetate

: 1052177-05-5
4-(2'-methylbut-3'-yn-2'-yloxy)phenyl acetate

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene; copper dichloride In acetonitrile at 0℃; for 18h;	80%

: 3233-32-7
hydroquinone monoacetate

: 63697-00-7
(S)-isopropyl lactate

: C14H18O5

Conditions

Conditions	Yield
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0 - 20℃; for 5h;	79%

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Hebei Nengqian Chemical Import and Export Co., LTD

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Hunan chemfish Pharmaceutical co.,Ltd

Hangzhou Dingyan Chem Co., Ltd

Antimex Chemical Limied

Hangzhou Fandachem Co.,Ltd

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Pure Chemistry Scientific Inc.

GZ HONESTCHEM CO., LTD

Wuxi Morality Chemical Co., Ltd

Sparrow Chemical Co.,Ltd

Shanghai Haoyuan Chemexpress Co., Ltd.

qingcang（shanghai） Medical Technology Co., Ltd.

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