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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172897Generated: October 31, 2026

Ammonium Hydroxide → 6-(Carbamoyl-fluoro-methyl)-benzo[b]thiophene-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1172897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
Reactant6-(Carboxy-fluoro-methyl)-benzo[b]thiophene-2-carboxylic acid ethyl esterHCID 59556412—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product6-(Carbamoyl-fluoro-methyl)-benzo[b]thiophene-2-carboxylic acid ethyl esterHCID 59556408—

Reaction Steps

To a slurry of 6-(carboxy-fluoro-methyl)-benzo[b]thiophene-2-carboxylic acid ethyl ester (400 mg, 1.42 mmol) in DCM (10 mL) was added oxalyl chloride (0.148 mL, 1.70 mmol) and 2 drops of DMF. After 20 min, the resultant solution was added to a solution of NH4OH (0.9 mL, 7.08 mmol) in DCM (5 mL) dropwise. After 1 h, the solvent was removed in vacuo and the solid was triturated with MeOH and H2O. The white solid was filtered and used without further purification. 1H NMR (DMSO-d6) δ 8.20 (s, 1H), 8.11 (s, 1H), 8.04 (d, J=8.2 Hz, 1H), 7.91 (br s, 1H), 7.62 (br d, J=2.4 Hz, 1H), 7.51 (d, J=8.2 Hz, 1H), 5.94 (d, J=45.7 Hz, 1H), 4.33 (q, J=7.2 Hz, 2H), 1.31 (t, J=7.2 Hz, 3H). cal'd 282 (MH+), exp 282 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834034B2
Source datasetuspto-grants-2010_11
ORD IDord-1472dfcd340246279a111007064c2267
Source noteuspto-grants-2010_11