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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442068Generated: October 31, 2026

Hydrochloric Acid → 4,4,6-Trimethylbicyclo[4.2.0]octan-2-ol

https://huagongshe.com/reaction/442068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantSodium borohydrideHCID 4311764—
Reactant4,4,6-Trimethylbicyclo[4.2.0]octan-2-oneHCID 22765515—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4,4,6-Trimethylbicyclo[4.2.0]octan-2-olHCID 645487597.5%

Reaction Steps

To a 2-liter 3-necked flask fitted with a mechanical stirrer, additional funnel, reflux condenser and drying tube was added 15 g. (0.39 mole) of sodium borohydride and 500 ml. 2-propanol. To this solution was slowly added 218.6 g. (1.317 moles) of 4,4,6-trimethylbicyclo[4.2.0]octane-2-one in 50 ml. of 2-propanol. After 2 hours, about 200 ml. of water was added. The mixture was stirred an additional 1 hour, then about 35 ml. concentrated hydrochloric acid was added. After another 1 hour of stirring, 400 ml. of toluene and 500 ml. of water were added. The layers were separated and the organic layer was washed three times with 100 ml. of water. The combined water layers were extracted with toluene. The toluene layers were combined and dried over potassium carbonate. The solution was concentrated in vacuo and the residue distilled through a 25 cm. Vigreux--column to yield 215.8 g. (1.284 moles, 97.5 % yield) of 4,4,6-trimethylbicyclo [4.2.0]octane-2-ol. IR: 3360 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044057
Source datasetuspto-grants-1977_08
ORD IDord-84cbe9df9c6f45aa82fa1b205f8e8cd5
Source noteuspto-grants-1977_08