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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693151Generated: October 30, 2026

Ammonium Chloride → [2-(3-Nitrophenyl)cyclohex-1-enyl]methanol

https://huagongshe.com/reaction/1693151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantCerium trichloride heptahydrateHCID 21585214—
Reactant2-(3-Nitrophenyl)cyclohex-1-enecarbaldehydeHCID 57827282—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product[2-(3-Nitrophenyl)cyclohex-1-enyl]methanolHCID 57827168—

Reaction Steps

Cerium chloride heptahydrate (1.22 g) was added to a mixed solution of 2-(3-nitrophenyl)cyclohex-1-enecarbaldehyde obtained in Preparation Example 4-(1) (630 mg) in methanol (60.0 mL) and THF (20.0 mL) in an ice bath. Sodium borohydride (130 mg) was added to the reaction solution at the same temperature, followed by stirring for 30 minutes. A saturated ammonium chloride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure to obtain a crude product. The resulting crude product was purified by NH-silica gel column chromatography to obtain the title compound (610 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158620B2
Source datasetuspto-grants-2012_04
ORD IDord-b565bedd4f7a4cba85a7b587ddd139dd
Source noteuspto-grants-2012_04