Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946541Generated: October 31, 2026

Water → 1-[(3,4-dichlorophenyl)methyl]-2-(1-methylethyl)-4,5,6,7-tetrahydro-1H-benzimidazol-7-ol

https://huagongshe.com/reaction/1946541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
Reactant3-[(3,4-dichlorophenyl)methyl]-2-(1-methylethyl)-3,5,6,7-tetrahydro-4H-benzimidazol-4-oneHCID 58460165—
SolventMethanolHCID 887—
Product1-[(3,4-dichlorophenyl)methyl]-2-(1-methylethyl)-4,5,6,7-tetrahydro-1H-benzimidazol-7-olHCID 58460236—

Reaction Steps

To Intermediate 80 (131.02 g, combination of two batches) under nitrogen in methanol (1000 mL) and dichloromethane (DCM) (1000 mL) was added sodium borohydride (29.4 g) slowly in portions over 10 min and the mixture stirred at room temperature under nitrogen. Temp rose from 19° C. to 23° C. Gas evolution still visible for 20-30 mins and temp rose over 40 mins to 26° C. Temp still going up after 1 hr20 min—now 26.2° C. After 2.5 hr water was added carefully and the mixture was partitioned between ethyl acetate and water (should have given the mixture more time to quench before extracting—gas evolution during extraction seen) and the aqueous layer extracted well with ethyl acetate. The combined organics were washed with water, brine, dried (MgSO4), filtered and evaporated. This gave the title compound, a white solid, 133.3 gm. LC/MS MH+ 339, 341, Rt 0.76 min (2 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399444B2
Source datasetuspto-grants-2013_03
ORD IDord-3745548e47be428dbc0e2042448ce194
Source noteuspto-grants-2013_03