HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074011Generated: November 2, 2026
Benzenesulfonyl chloride → HCID 14858872, compound
https://huagongshe.com/reaction/1074011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 14858903 | HCID 14858903 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14858872 | HCID 14858872 | 90.6% |
Reaction Steps
L-seryl-L-proline benzylester hydrochloride (1.64 g, 5 mmole) was dissolved in methylene chloride (30 ml), and triethylamine (1.11 g, 11 mmole) was added thereto at -30° C. Methylene chloride (10 ml) solution of benzene sulfonyl chloride (0.86 g, 5 mmole) was added dropwise thereto. The mixture was stirred for 1 hour at less than 0° C. and then for 5 hours at room temperature, and methylene chloride (60 ml) was added thereto. The mixture was washed with 5% aqueous sodium bicarbonate (100 ml, twice), 1N aqueous hydrochloric acid (100 ml, twice) and water (100 ml) in the order given, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain N-benzenesulfonyl-L-seryl-L-proline benzylester (yield: 1.96 g, 90.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04971993 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-95b42ba418834c9784eca65b5630c66d |
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| Source note | uspto-grants-1990_11 |
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