Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788943Generated: November 1, 2026

Sodium hydride → HCID 13363535, compound

https://huagongshe.com/reaction/1788943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzenesulfenyl chlorideHCID 11008040—
ReactantHCID 13363515HCID 13363515—
SolventDimethylformamideHCID 6228—
ProductHCID 13363535HCID 1336353587.6%

Reaction Steps

Sodium hydride (0.107 g; 60% dispersion in mineral oil) was dispersed in N,N-dimethylformamide (20 ml). To this solution was added isopropyl N-(8-ethoxy-1,3-benzodioxan-6-yl)carbamate (0.75 g) under ice-cooling. After being stirred at room temperature for 1 hour, phenylsulfenyl chloride (0.39 g) was added thereto under ice-cooling, and stirring was continued at room temperature overnight. The resulting mixture was poured into ice-water and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography using a mixture of toluene and ethyl acetate as the eluent to give isopropyl N-phenylthio-N-(8-ethoxy-1,3-benzodioxan-6-yl)carbamate (Compound 25) (0.91 g) in a yield of 87.5%. M.P., 120°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686232
Source datasetuspto-grants-1987_08
ORD IDord-323422090e9547dfb62757ce11acaab4
Source noteuspto-grants-1987_08