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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492469Generated: October 31, 2026

Water → HCID 10760318, compound

https://huagongshe.com/reaction/1492469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
Reactant(1S,2S)-Cyclohex-4-ene-1,2-diyldimethanolHCID 10942538—
SolventPyridineHCID 1049—
ProductHCID 10760318HCID 10760318100%

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzoyl chloride (2.0 ml, 17 mmoles) was slowly added to a solution of (4S,5S)-4,5-bis(hydroxymethyl)-1-cyclohexene (1.00 g, 7.0 mmoles) in pyridine (7 ml) while cooling the system with ice. The resulting mixture was stirred at 0° C. for one hour. After adding dimethylaminopropylamine (0.8 ml, 6.4 mmoles) to the reaction mixture and stirring it at that temperature for 15 minutes, water was added and the product formed was extracted with ethyl ether. The ether extract solution was washed successively with water, dilute hydrochloric acid and saturated aqueous solution of sodium chloride and then dried on anhydrous sodium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:9, v/v) to obtain (4S,5S)-4,5-bis(benzoyloxymethyl)- 1-cyclohexene (2.5 g, Yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374625
Source datasetuspto-grants-1994_12
ORD IDord-71e00abd61f74767aa19545b28eac555
Source noteuspto-grants-1994_12