HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728421Generated: October 29, 2026
Ethyl Acetate → (R)-4-(Methylthio)-2-(methanesulfonyloxy)butyl Methanesulfonate
https://huagongshe.com/reaction/1728421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (R)-4-(methylthio)1,2-butanediol | HCID 10920564 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (R)-4-(Methylthio)-2-(methanesulfonyloxy)butyl Methanesulfonate | HCID 14634096 | — |
Reaction Steps
(R)-4-(Methylthio)-1,2-butanediol (0.47 g, 3.4 mmol) was dissolved in 5 ml of pyridine and cooled to 0° C. Methanesulfonyl chloride (0.66 ml, 8.5 mmol) was added and the mixture stirred for 2 hours while warming to room temperature, by which time tlc (ethyl acetate) indicated complete conversion of starting material (Rf 0.4) to title product (Rf 0.85). The reaction mixture was diluted with 10 ml H2O and extracted 2×15 ml of ethyl acetate. The organic layers were combined, dried (MgSO4) and stripped to in vacuo to yield title product an an oil, all of which was used in the next step; tlc Rf 0.85 (ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05326884 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-3138851051864a529026910e7967dab3 |
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| Source note | uspto-grants-1994_07 |
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