Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406832Generated: October 31, 2026

Hydrochloric Acid → HCID 178520929, compound

https://huagongshe.com/reaction/1406832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178520928HCID 178520928—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178520929HCID 17852092997.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

Then, trans-4-(3,5-difluorophenyl)cyclohexane carbaldehyde (112 g) was dissolved in ethanol (224 mL), THF (30 mL), and water (30 mL), and sodium tetrahydroborate (9.4 g) was slowly added to the resultant solution at an outside temperature or 5° C., followed by stirring at an outside temperature of 5° C. for 10 minutes. The reaction solution was slowly poured into 10% hydrochloric acid (450 mL) and stirred for a white, and then an organic layer was separated. An aqueous layer was subjected to extraction with ethyl acetate, and the ethyl acetate extract was combined with the organic layer and washed with saturated brine two times. The mixture was dried with anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure to yield 110 g of trans-4-(3,5-difluorophenyl)cyclohexylmethanol as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916718B2
Source datasetuspto-grants-2014_12
ORD IDord-0a4a11fac3064a18a8805862b4c684b1
Source noteuspto-grants-2014_12