HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428369Generated: October 25, 2026
Sodium methanethiolate → HCID 66609952, compound
https://huagongshe.com/reaction/1428369
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl ester | HCID 57466610 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66609952 | HCID 66609952 | 100.2% |
Reaction Steps
Sodium methanethiolate (4.36 g, 62.30 mmol) was added to a stirred solution of ethyl 1-((methylsulfonyloxy)methyl)cyclopropanecarboxylate (6.92 g, 31.10 mmol) in N,N-dimethylformamide (62.30 mL) at 23° C. The resulting brown suspension was stirred at 23° C. for 18 h. The reaction mixture was diluted with water and extracted with diethyl ether. The combined organic layers were dried (MgSO4), filtered, and concentrated by rotary evaporation to afford the title compound as a brown oil (5.43 g, 100%): 1H NMR (300 MHz, CDCl3) δ 4.14 (q, J=7 Hz, 2H), 2.83 (s, 2H), 2.16 (s, 3H), 1.31 (dd, J=7, 4 Hz, 2H), 1.25 (t, J=7 Hz, 3H), 0.89 (dd, J=7, 4 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08937083B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-4862283495ec41f0b40db9844882e78a |
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| Source note | uspto-grants-2015_01 |
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