HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591784Generated: October 30, 2026
Acetyl chloride → 4-Acetyl-2,6-dimethoxyphenyl acetate
https://huagongshe.com/reaction/1591784
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetosyringone | HCID 17198 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Acetyl-2,6-dimethoxyphenyl acetate | HCID 3015410 | 99% |
Reaction Steps
3.0 g (15.3 mmol) of 3,5-dimethoxy-4-hydroxyacetophenone is dissolved in dichloromethane (30 ml) and 2.53 g (18.3 mmol) of K2CO3 is added. Triethylamine (2.6 ml) is then added dropwise. The reaction medium is cooled down to 0° C. and acetyl chloride (1.31 ml; 18.3 mmol) is added. The mixture is stirred for 24 hours at ambient temperature then poured into ice-cooled water. After extraction with dichloromethane, the organic phase is washed with sodium chloride in a saturated aqueous solution before being dried over magnesium sulphate, filtered and concentrated under vacuum. The product obtained is purified by crystallization from ether in order to produce a white solid with a yield of 99%. Melting point: 145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07291641B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-f06e4c00fecf43ed9d8cb6b4e74b5522 |
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| Source note | uspto-grants-2007_11 |
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