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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232608Generated: October 30, 2026

Hydrochloric Acid → (1r,5s)-6,6-Dimethyl-3-oxabicyclo[3.1.0]hexan-2-one

https://huagongshe.com/reaction/2232608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantSodium CarbonateHCID 10340—
ReactantSodium borohydrideHCID 4311764—
Reactant(1R, 4R, 5S) 4-Hydroxy-6,6-dimethyl-3-oxabicyclo(3.1.0)hexan-2-oneHCID 10931532—
SolventWaterHCID 962—
Product(1r,5s)-6,6-Dimethyl-3-oxabicyclo[3.1.0]hexan-2-oneHCID 1109462086%

Reaction Conditions

Temperature0 °C

Reaction Steps

170.6 g of (1R,5S) 6,6-dimethyl-4-(R)-hydroxy-3-oxa-bicyclo (3,1,0) hexane-2-one were added to 800 ml of water and a solution of 127.2 g of sodium carbonate in 400 ml of water was slowly added thereto at 0° C. The mixture was stirred at 0° C. for 15 minutes and 45.4 g of sodium borohydride were added thereto at 0° C. in small fractions. The mixture was stirred for 4 hours at 0° C. and adjusted to a pH of 2 by addition of 2N hydrochloric acid. The mixture was saturated with sodium chloride and stood overnight and was extracted with methylene chloride. The extract was evaporated to dryness under reduced pressure and the residue was rectified under reduced pressure to obtain 130.2 g of (1R,5S) 6,6-dimethyl-3-oxa-bicylo (3,1,0) hexane-2-one with a specific rotation of [α]D20 =-92° (c=1% in ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788305
Source datasetuspto-grants-1988_11
ORD IDord-d4b08777325d4a06ad9a95805458df71
Source noteuspto-grants-1988_11