Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946472Generated: November 2, 2026

Sodium borohydride → 3-[(4-Chlorophenyl)methyl]-2-(1-methylethyl)-3,4,5,6,7,8-hexahydrocyclohepta[d]imidazol-4-ol

https://huagongshe.com/reaction/1946472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-[(4-chlorophenyl)methyl]-2-(1-methylethyl)-5,6,7,8-tetrahydrocyclohepta[d]imidazol-4(3H)-oneHCID 58460226—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product3-[(4-Chlorophenyl)methyl]-2-(1-methylethyl)-3,4,5,6,7,8-hexahydrocyclohepta[d]imidazol-4-olHCID 5846022589%

Reaction Steps

Sodium borohydride (100 mg) was added to a stirred solution of Intermediate 3 (420 mg) in dichloromethane (3 ml) and methanol (3.00 ml). The reaction mixture was stirred for 1 hour. The reaction mixture was partitioned between EtOAc (50 ml) and water (30 ml). The two phases were separated and the aqueous phase was extracted again with EtOAc (30 ml). The phases were separated, the organic extracts were combined, dried (hydrophobic frit) and concentrated under vacuum to give the title compound (376 mg). LC/MS MH+ 319, Rt 0.77 min (2 minute run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399444B2
Source datasetuspto-grants-2013_03
ORD IDord-9e4f903e09dd4b358eb9df5806a75c35
Source noteuspto-grants-2013_03