HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250864Generated: October 30, 2026
Benzenesulfonyl chloride → HCID 57041896, compound
https://huagongshe.com/reaction/1250864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid | HCID 69922785 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57041896 | HCID 57041896 | — |
Reaction Steps
224.5 mg of 4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid were dissolved in 2 ml of DMF and cooled to 0° C. 207 mg of benzenesulfonyl chloride and 303 mg of diisopropylethylamine were added and the reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was cooled to −25° C. for 16 hours and then warmed to room temperature. The reaction was quenched by the addition of water, and the mixture was extracted three times with dichloromethane. The combined organic phases were dried with sodium sulfate, filtered and the solvent was removed in vacuo. The residue was chromatographed on silica gel eluting with dichloromethane/methanol/water/acetic acid (9/1/0.1/0.1). Yield 98 mg. MS (ES+): m/e=464.1 (M+H)+; 408.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06340679B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-18f9cfacb862436ebe47848c4cde73a6 |
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| Source note | uspto-grants-2002_01 |
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