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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337790Generated: October 27, 2026

Ammonium Chloride → 2-(1-Methyl-1h-imidazol-5-yl)cyclohexan-1-ol

https://huagongshe.com/reaction/337790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(3-Methylimidazol-4-yl)cyclohex-2-en-1-oneHCID 89963299—
SolventMethanolHCID 887—
Product2-(1-Methyl-1h-imidazol-5-yl)cyclohexan-1-olHCID 8996339861.1%

Reaction Steps

To a solution of the 2-(1-methyl-1H-imidazol-5-yl)cyclohex-2-en-1-one (80 mg, 0.454 mmol) prepared in Example 49a in methanol (2.0 mL), sodium borohydride (50 mg, 1.32 mmol) was added at room temperature, and the reaction solution was stirred at room temperature for 30 minutes. To the reaction solution, a saturated aqueous solution of ammonium chloride (20 mL) was added, followed by extraction with dichloromethane (50 mL). The thus obtained organic layer was dried over anhydrous sodium sulfate and vacuum concentrated to yield the title compound (50 mg, 61%) in the form of a trans/cis (2:1) mixture as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889741B2
Source datasetuspto-grants-2014_11
ORD IDord-cb02b9af030046f4bfa6394f54e31ca1
Source noteuspto-grants-2014_11