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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747322Generated: October 31, 2026

Hydrochloric Acid → 1-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-one

https://huagongshe.com/reaction/1747322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant1,4-DioxaneHCID 31275—
Reactant1-Isopropenyl-3-(4-methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-oneHCID 59497427—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product1-(4-Methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-oneHCID 59497379100.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

1-Isopropenyl-3-(4-methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-one (630 mg, 1.9 mmol) is dissolved in methanol (2.0 mL), 1,4-dioxane (10 mL) and water (2.0 mL). Then 37% HCl (1.6 mL) is added and the reaction mixture is heated at 65° C. for 6 hr. A white solid is formed during the heating. Then water (80 mL) and CH2Cl2 (80 mL) are added. The organic layer is separated and the aqueous layer is extracted with CH2Cl2 (3×50 mL). The organic layers are combined, washed with Sat. NaHCO3 (100 mL), Sat. NH4Cl (100 mL) and water (3×100 mL), dried over MgSO4 and concentrated to give 560 mg (99%) of 1-(4-methyl-benzo[b]thiophen-3-ylmethyl)-1,3-dihydro-benzimidazol-2-one which is used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150556B2
Source datasetuspto-grants-2015_10
ORD IDord-20bc20d469ac4646883388ce71cf3c69
Source noteuspto-grants-2015_10