HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458375Generated: October 29, 2026
Potassium ethanethioate → (3s,5r)-Thioacetic acid s-[5-benzyloxymethyl-1-(naphthalene-2-sulfonyl)-pyrrolidin-3-yl] ester
https://huagongshe.com/reaction/458375
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | (3S,5S)-methanesulfonic acid 5-benzyloxymethyl-1-(naphthalene-2-sulfonyl)-pyrrolidin-3-yl ester | HCID 87832403 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3s,5r)-Thioacetic acid s-[5-benzyloxymethyl-1-(naphthalene-2-sulfonyl)-pyrrolidin-3-yl] ester | HCID 88052672 | 75.2% |
Reaction Steps
To a solution of (3S,5S)-methanesulfonic acid 5-benzyloxymethyl-1-(naphthalene-2-sulfonyl)-pyrrolidin-3-yl ester (3.0 g) in abs DMF (60 ml) was added potassium thioacetate (1.08 g). The reaction mixture was stirred for 1 h at 100° C. and concentrated under oil pump vacuum. The residue was treated with ice/water and extracted with EtOAc. The organic phase was washed with water and brine, dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel using EtOAc/hexane 1:3 as eluent to obtain (3S,5R)-thioacetic acid S-[5-benzyloxymethyl-1-(naphthalene-2-sulfonyl)-pyrrolidin-3-yl] ester (2.16 g) as a slightly yellow powder, MS: 334 (M-121).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189756B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-031ab89c9476414eb08803c3b44a09f9 |
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| Source note | uspto-grants-2007_03 |
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