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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530176Generated: November 2, 2026

Ammonium Chloride → HCID 178444289, compound

https://huagongshe.com/reaction/1530176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178444288HCID 178444288—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178444289HCID 178444289199.9%

Reaction Steps

Under a nitrogen atmosphere, 4.0 g of 4-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-2-cyclohexenone (r-9) was dissolved into 50 mL of THF, 14.5 mL of butylmagnesium bromide THF solution (1 M/L) was added dropwise thereto at room temperature, and the resultant mixture was stirred at 50° C. for 30 minutes, and then stirred at room temperature overnight. A saturated aqueous solution of ammonium chloride was added dropwise under ice-cooling, the resultant mixture was subjected to extraction with ethyl acetate, and then organic layers were combined, the resultant organic layer was washed with saturated brine, and then dried over anhydrous magnesium sulfate. A solvent was evaporated under reduced pressure, and the resultant residue was purified by fractionation on silica gel column chromatography (eluate:heptane:ethyl acetate=7:3 (in a volume ratio)), and thus 4.70 g of 4-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-1-butyl-2-cyclohexene-1-ol (compound (r-10)) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090825B2
Source datasetuspto-grants-2015_07
ORD IDord-491872625f784f908dd7338548592da6
Source noteuspto-grants-2015_07