HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859452Generated: November 1, 2026
Triethylamine → (S)-1-(4-dimethylaminophenethyl)-3-methanesulfonyloxy-pyrrolidine
https://huagongshe.com/reaction/1859452
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (S)-1-(4-dimethylaminophenethyl)-3-hydroxypyrrolidine | HCID 69900648 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-1-(4-dimethylaminophenethyl)-3-methanesulfonyloxy-pyrrolidine | HCID 86585524 | — |
Reaction Steps
(S)-1-(4-dimethylaminophenethyl)-3-hydroxypyrrolidine (320 mg, 1.37 mmol) was dissolved in dichloromethane (10 ml). Triethylamine (152 mg, 1.50 mmol) and methanesulfonyl chloride (164 mg, 1.43 mmol) were added to the obtained solution under stirring under cooling on ice. They were stirred at 0° C. for 1 hour. The reaction liquid was distributed in dichloromethane and water. The organic layer was dried, and the solvent was evaporated under reduce pressure. The obtained residue was subjected to silica gel column chromatography. The product was eluted with dichloromethane and then with a solvent mixture (50:1) of dichloromethane and methanol. The appropriate fractions were combined, and the solvent was evaporated under reduced pressure to obtain (S)-1-(4-dimethylaminophenethyl)-3-methanesulfonyloxy-pyrrolidine in the form of a light yellow oil (378 mg, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06528504B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-a6aea6b868d242b8895442c66ea8c458 |
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| Source note | uspto-grants-2003_03 |
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