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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324504Generated: October 29, 2026

Sodium hydrosulfide → HCID 88151774, compound

https://huagongshe.com/reaction/324504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrosulfideHCID 28015—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178503574HCID 178503574—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 88151774HCID 88151774—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of the product of example 39 step (i) (0.120 g) together with 2-bromoethyl methyl ether (0.073 ml) and a 1M solution of potassium tert-butoxide in tetrahydrofuran (0.62 ml) in N,N-dimethylformamide (3 ml) was heated at 50° C. for 20 h. Sufficient sodium hydrosulphide was added to give a blue solution and the reaction mixture heated at 80° C. for 4 h. The reaction mixture was cooled, diluted with ethyl acetate and washed with saturated aqueous ammonium chloride. The organic phase was dried over magnesium sulphate, filtered and evaporated. The crude product was purified by chromatography eluting with 1% methanol in dichloromethane, followed by trituration with ethyl acetate to give the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218376B1
Source datasetuspto-grants-2001_04
ORD IDord-7bd2ca4f6b7a4e06a8ac7f7d38531727
Source noteuspto-grants-2001_04