Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835171Generated: November 1, 2026

Ammonium Chloride → HCID 23503239, compound

https://huagongshe.com/reaction/1835171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantN,2-dimethoxy-N-methylacetamideHCID 14872187—
Reactant5-[(3-Chlorophenyl)methyl]4-{2-[(1,1-dimethylethyl)dimethylsilyl]oxyethoxy}thiophene-3-carboxylic acidHCID 23503231—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23503239HCID 23503239—

Reaction Conditions

Temperature-20 °C

Reaction Steps

2.0M butyl lithium in hexanes (1 ml) was diluted with tetrahydrofuran (3 ml) and cooled to −20° C. 5-[(3-Chlorophenyl)methyl]-4-{2-[(1,1-dimethylethyl)-dimethylsilyl]oxyethoxy}thiophene-3carboxylic acid in tetrahydrofuran (1 ml of 1M solution) was added slowly. The solution was mixed for 10 minutes and then 1 mmol of 2,N-Dimethoxy-N-methylacetamide in 1 ml of tetrahydrofuran was added. The solution was mixed for 10 minutes and was then added to 5 m of ammonium chloride solution. The reaction mixture was evaporated in air for 18 hours. The residue was dissolved in dichloromethane and washed with water twice. The solvent was allowed to evaporate and the residue was then dissolved in 5 ml of ethanol. To this solution was added 92 mg of methyl hydrazine. The resulting solution was heated at reflux for 4 hours. The reaction mixture was allowed to cool and the solvent was evaporated. Purification by column chromatography, eluting with an isohexane:ethyl acetate gradient, gave the title compound (4 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770646B2
Source datasetuspto-grants-2004_08
ORD IDord-23425716865a402f82835d1bca90cbb3
Source noteuspto-grants-2004_08