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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747328Generated: October 26, 2026

Methanol → 3-[3-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester

https://huagongshe.com/reaction/1747328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantEthyl trans-2-hexenoateHCID 5364778—
Reactant1-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-oneHCID 59497379—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-[3-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl esterHCID 5949761795%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-one (50 mg, 0.17 mmol) in dry DMF (1.0 mL) are added (E)-Hex-2-enoic acid ethyl ester (27 mg, 0.19 mmol) and 40% benzyltrimethyl ammonium hydroxide in MeOH (0.008 mL, 0.017 mmol). The resulting mixture is warmed up to 60° C. for 16 hr. Then another 27 mg of (E)-Hex-2-enoic acid ethyl ester is added the heating is continued for another 8 hr. Then saturated NH4Cl (2 mL) and water (10 mL) are added and the mixture is extracted with EtOAc (3×25 mL). The organic layers are combined, dried over MgSO4 and concentrated to give the crude product. Purification with flash column chromatography using 20% EtOAc in Hexanes affords 70 mg (95%) of 3-[3-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-2-oxo-2,3-dihydro-benzimidazol-1-yl]-hexanoic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150556B2
Source datasetuspto-grants-2015_10
ORD IDord-73fcba765c7348dc976c9e08883714bf
Source noteuspto-grants-2015_10