Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328763Generated: November 1, 2026

Methanethiol → HCID 86735331, compound

https://huagongshe.com/reaction/328763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 86735331HCID 8673533158%

Reaction Steps

Methyl mercaptan (excess) is passed into a rapidly stirred solution of sodium methoxide (13.5 g., 0.25 mole) in dry methanol (200 ml.) at 0° C. to generate sodium methylmercaptide. The resulting solution is treated with dimethyl 2-bormoazelate (55.0 g., 0.186 mole), then stirred and heated at reflux under nitrogen for 5 hours. The reaction solution is concentrated in vacuo, diluted with ether and filtered. The filtrate is washed with water (until the washings are neutral), dried over sodium sulfate and distilled providing the title compound as a colorless liquid (28.4 g., 58%), bp 0.2 mm 128°-138° C.; pmr (CDCl3) δ 2.10 (s, 3H), 2.31 (t,2H), 3.20 (t,H), 3,63 (s,3H) and 3.71 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04018802
Source datasetuspto-grants-1977_04
ORD IDord-1b77f7f19b544a47987bf2637841d0a8
Source noteuspto-grants-1977_04