HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251906Generated: November 1, 2026
Triethylamine → (S)-3-methanesulfonyloxy-1-(3-pyrrolidinophenethyl)pyrrolidine
https://huagongshe.com/reaction/2251906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (S)-3-hydroxy-1-(3-pyrrolidinophenethyl)pyrrolidine | HCID 69199429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-3-methanesulfonyloxy-1-(3-pyrrolidinophenethyl)pyrrolidine | HCID 86592731 | — |
Reaction Steps
(S)-3-Hydroxy-1-(3-pyrrolidinophenethyl)pyrrolidine (1.04 g, 4.00 mmol) was dissolved in dichloromethane (10 ml). Triethylamine (0.76 ml, 5.49 mmol) and methanesulfonyl chloride (0.39 ml, 5.03 mmol) were added to the obtained solution at 0° C. and they were stirred overnight. The reaction mixture was distributed into 5% aqueous sodium hydrogencarbonate solution and dichloromethane. The organic layer was dried and the solvent was evaporated under reduced pressure. The residue was subjected to the silica gel column chromatography. After the elution with chloroform and methanol (95:5), suitable fractions were collected and the solvent was evaporated under reduced pressure to obtain (S)-3-methanesulfonyloxy-1-(3-pyrrolidinophenethyl)pyrrolidine in the form of a light yellow oily substance (1.30 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07320973B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-c4f2ec73e38447bb8eff78300736474a |
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| Source note | uspto-grants-2008_01 |
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