HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074007Generated: October 30, 2026
Benzenesulfonyl chloride → N-benzenesulfonyl-L-prolyl-L-proline benzylester
https://huagongshe.com/reaction/1074007
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-prolyl-L-proline benzylester hydrochloride | HCID 14827459 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-benzenesulfonyl-L-prolyl-L-proline benzylester | HCID 14858868 | 98.1% |
Reaction Steps
L-prolyl-L-proline benzylester hydrochloride (1.69 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 to the solution. The mixture was stirred for 1 hour at less than 0° C., and next for 5 hours at room temperature, and methylene chloride (60 ml) was added thereto. The solution 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-prolyl-L-proline benzylester(yield: 2.17 g, 98.1%)
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-834c746514464b538d85ad86b4e593ed |
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| Source note | uspto-grants-1990_11 |
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