HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26679Generated: October 27, 2026
Acetyl chloride → Methyl 2-(3-acetyl-4-hydroxyphenyl)propionate
https://huagongshe.com/reaction/26679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Methyl 2-(4-methoxyphenyl)propanoate | HCID 12398855 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(3-acetyl-4-hydroxyphenyl)propionate | HCID 21322000 | — |
Reaction Steps
Titanium tetrachloride (82.3 mls) was added dropwise to a stirred solution of methyl 2-(4-methoxyphenyl)propionate (25 g) in dry dichloromethane (250 mls), cooled in an ice/salt-bath, at a rate sufficient to maintain the temperature between -10° C. and -5° C. The mixture was stirred for 10 minutes and acetyl chloride (10 g) was added dropwise at a rate sufficient to maintain the temperature below 0° C. The solution was stirred at -5° C. for 11/2 hours when boron trichloride (15 mls) was added. Stirring was continued for 1/2 hour at +3° C. before pouring on to crushed ice/concentrated hydrochloric and separating the two phases. The aqueous phase was extracted with ether (3x) and the combined organic extracts were washed with saturated sodium bicarbonate solution, saturated brine solution, and dried over anhydrous magnesium sulphate. Evaporation of the solvent yielded the crude product as a pale yellow oil. Vacuum distillation furnished a pale yellow oil bp 120°-125° C./0.15 mm (16.2 g; 59%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04151179 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-ab2ce73424b541b4a81672a916ba67f8 |
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| Source note | uspto-grants-1979_04 |
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