Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521593Generated: October 30, 2026

Ethanethiol → HCID 70977846, compound

https://huagongshe.com/reaction/1521593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57885697HCID 57885697—
SolventDimethylformamideHCID 6228—
ProductHCID 70977846HCID 70977846—

Reaction Steps

To a cooled (0° C.) solution of sodium hydride (60% dispersion in mineral oil, 0.094 g, 2.35 mmol) in N,N-dimethylformamide (9.4 mL) was added ethanethiol (0.140 mL, 1.88 mmol). The reaction was warmed to room temperature and stirred for 30 minutes. It was then cooled to 0° C., and a solution of the title compound from Example 62 Step A (0.250 g, 0.939 mmol) in N,N-dimethylformamide (1 mL) added. The resulting solution stirred at room temperature until the reaction was complete. The reaction was then quenched with water and extracted with ethyl acetate. The combined organic extracts were washed with water and saturated aqueous sodium chloride solution, dried, filtered and concentrated under reduced pressure. Purification by flash chromatography on silica gel (0-60% ethyl acetate in hexanes) provided the title compound: LCMS m/z 233.91 [M+2+H]+; 1H NMR (500 MHz, CDCl3) δ 8.50 (s, 1H), 8.39 (s, 1H), 7.79 (s, 1H), 3.62 (s, 2H), 2.39 (q, J=7.4, 2H), 1.19 (t, J=7.4, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073929B2
Source datasetuspto-grants-2015_07
ORD IDord-3facb623e2b44941aa8adeb881e56bed
Source noteuspto-grants-2015_07