HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957939Generated: October 30, 2026
Ethyl phenylacetate → (4-Chlorosulfonyl-phenyl)-acetic acid ethyl ester
https://huagongshe.com/reaction/1957939
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl phenylacetate | HCID 7590 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | (4-Chlorosulfonyl-phenyl)-acetic acid ethyl ester | HCID 10467900 | 56.3% |
Reaction Steps
The chlorosulfonic acid (16.6 mL, 250 mmol) was added dropwise into ethyl phenylacetate (8.2 g, 50 mmol) under stirring at 40° C. Thereafter, the mixture was stirred for 0.5 hour at room temperature, and then poured on ice and extracted with dichloromethane. The combined organic phase was washed by saline, dried with sodium sulfate and concentrated under reduced pressure. The concentrate was separated through column chromatography (petroleum ether/ethyl acetate=6/1, v/v) to obtain yellow oil (7.4 g, yield: 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410094B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-9bd4a204d30d43f1acb4bd26ce5b8560 |
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| Source note | uspto-grants-2013_04 |
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