HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742055Generated: October 26, 2026
Ethanethiol → Ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate
https://huagongshe.com/reaction/742055
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | Ethyl 2-[[4-methoxybenzenesulfonyl](isobutyl)amino]acetate | HCID 10640094 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate | HCID 10591435 | — |
Reaction Steps
A solution of ethanethiol (15 mL) and methylene chloride (15 mL) is cooled to 0° C. Aluminum trichlofide (9.62 g, 72.2 mmol) is added (the solution turns green), and the reaction is warmed to room temperature. Ethyl 2-[[4-methoxybenzenesulfonyl](isobutyl)-amino]acetate (4.75 g, 14.44 mmol) is added in methylene chloride (5 mL), and the reaction is stirred for 3.5 hours at room temperature. The reaction is then slowly quenched with water, and the crude reaction is partitioned between water and methylene chloride. The aqueous layer is extracted well with methylene chloride, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (25% to 50% ethyl acetate/hexane) to give ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05552419 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-9afe8ac81c8e40299b0c193456aa3049 |
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| Source note | uspto-grants-1996_09 |
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