HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250862Generated: October 31, 2026
4-Chlorobenzenesulfonyl chloride → HCID 69920461, compound
https://huagongshe.com/reaction/1250862
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| 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 69920461 | HCID 69920461 | — |
Reaction Steps
200 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. 220 mg of 4-chlorobenzenesulfonyl chloride and 270 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 84 mg. MS (ES+): m/e=498.1 (M+H)+; 442.1.
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-50f4375e25f64d2e8bea1670f24dbc54 |
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| Source note | uspto-grants-2002_01 |
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