Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682121Generated: October 30, 2026

Ethanethiol → HCID 178477456, compound

https://huagongshe.com/reaction/1682121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178475771HCID 178475771—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178477456HCID 17847745637.6%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a 0° C. suspension of NaH (60% oil dispersion, 200 mg, 498 mmol) in THF (20 ml) was added ethanethiol (0.37 mL, 4.98 mmol). The resultant mixture was stirred for 10 min, cooled to -20° C., and compound 13 (1.9g, 3.83 mmol) was added. The solution was stirred further for 30 min at room temperature and concentrated. The residue was partitioned between ethyl acetate and pH 7.0 aqueous buffer. The organic phase was washed with brine, dried (Na2SO4), and concentrated. The residue was purified by silica gel chromatography (Et2O) to afford 718 mg (36%) of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175283
Source datasetuspto-grants-1992_12
ORD IDord-9a5c13ccf3ec4afa9b7027654fc39aec
Source noteuspto-grants-1992_12