HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385442Generated: October 27, 2026
Diethyl Ether → Ethyl 3-chloro-4-hydroxyphenylacetate
https://huagongshe.com/reaction/385442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Ethyl 4-hydroxyphenylacetate | HCID 28310 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-chloro-4-hydroxyphenylacetate | HCID 11031224 | 59.2% |
Reaction Steps
To a stirred solution of ethyl 2-(4-hydroxyphenyl)acetate (25 g, 138 mmol) in 375 ml of DCM, sulfuryl chloride (9.48 mL 118 mmol) was slowly added at 0° C. over a period of 30 min. Diethyl ether (19.6 mL) was slowly added reaction mixture at 0° C. and stirring was continued for 30 min at 0° C. The reaction mixture was slowly warmed to 15° C. for 1 h. After completion of reaction, the mixture was poured onto crushed ice and extracted with DCM (×2). The combined organic layers were washed with 10% NaHCO3 solution followed by water. The organic layer was dried over Na2SO4, filtered and evaporated under vacuum to give compound ethyl 2-(3-chloro-4-hydroxyphenyl)acetate (15 g) as a thick oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367863B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-485475320eee40bf8bfcba4c319b3988 |
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| Source note | uspto-grants-2013_02 |
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