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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226852Generated: October 31, 2026

Ammonium Hydroxide → HCID 10490982, compound

https://huagongshe.com/reaction/2226852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-[(1-Methylethyl)thio]benzo[b]thiophene-2-carboxylic acidHCID 13961669—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10490982HCID 1049098283%

Reaction Steps

To 3-[(1-methylethyl)thio]benzo[b]thiophene-2-carboxylic acid (133 mg, 0.53 mmol) [Connor D. T., et al., U.S. Pat. No. 4,703,053 (1987)] in 6 mL of THF is added N,N-carbonyldiimidazole (99 mg, 0.61 mmol). The mixture is heated at reflux for 1.5 hours then cooled slightly. Aqueous NH4OH (1 mL) is added and the reaction mixture is stirred at room temperature for 30 minutes, then partitioned between ethyl acetate and brine. The organic layer is dried over MgSO4, filtered, and concentrated in vacuo. The crude product is purified by flash chromatography eluting with 1:1 hexane:ethyl acetate to provide 3-[(1-methylethyl)thio]benzo[b]thiophene-2-carboxamide in 83% yield; mp=183-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350748
Source datasetuspto-grants-1994_09
ORD IDord-cdae854420d048bea78cb25c63a3e8af
Source noteuspto-grants-1994_09