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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (1R, 4R, 5S) 4-Hydroxy-6,6-dimethyl-3-oxabicyclo(3.1.0)hexan-2-one | HCID 10931532 | — |
| Solvent | Water | HCID 962 | — |
| Product | (1r,5s)-6,6-Dimethyl-3-oxabicyclo[3.1.0]hexan-2-one | HCID 11094620 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04788305 |
|---|
| Source dataset | uspto-grants-1988_11 |
|---|
| ORD ID | ord-d4b08777325d4a06ad9a95805458df71 |
|---|
| Source note | uspto-grants-1988_11 |
|---|