HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276355Generated: October 30, 2026
Methanesulfonyl chloride → HCID 54252157, compound
https://huagongshe.com/reaction/1276355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 54574124 | HCID 54574124 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54252157 | HCID 54252157 | 66.2% |
Reaction Steps
(S)-1-(tert-Butoxycarbonylamino)-3-hydroxypyrrolidine (40 g, 0.21 mol) was dissolved in anhydrous methylene chloride (400 mL), in the presence of N,N-diisopropyl-ethylamine (73 mL, 0.42 mol, 2 equiv.) and cooled using an ice bath. This solution was treated with methanesulfonyl chloride (18 mL, 0.23 mol, 1.1 equiv.) over a 30 min. period and was then allowed to stir at room temperature for 4 h. The solution was concentrated and the residue dissolved in ethyl acetate (250 mL). The resulting organic solution washed with 5% NaHCO3 and then with brine. The organic extract was dried over magnesium sulfate, filtered and concentrated to give (S)-1-(tert-butoxycarbonyl-amino)-3-methanesulfonyloxypyrrolidine as a dark oil (39 g) which was used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166015 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-7da3e2c48dc649e2b179432fa4cda875 |
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| Source note | uspto-grants-2000_12 |
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