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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425309Generated: October 28, 2026

Acetone → HCID 22463177, compound

https://huagongshe.com/reaction/2425309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBorohydrideHCID 28123—
ReactantSodium borohydrideHCID 4311764—
Reactant2,4,7-trimethyl-1-indanoneHCID 11095121—
SolventEthanolHCID 702—
ProductHCID 22463177HCID 22463177100%

Reaction Conditions

Temperature0 °C

Reaction Steps

8.95 g of 2,4,7-trimethylindanone (51.4 mmol) were dissolved in 70 ml of EtOH; the solution was cooled to 0° C. and 2.00 g of NaBH4 (51.8 mmol) were added to it in small aliquots. At the end of the addition, the reaction mixture was allowed to reach ambient temperature and then heated at 50° C. for 3 hours and 30 min. The reaction mixture was cooled to 0° C., and 50 ml of acetone were slowly (careful: exothermic reaction!) added to it to deactivate the residual borohydride. All volatiles were then removed in vacuo, the white solid obtained was treated with 50 ml of 1H2O and stirred for 30 min. The organic layer was extracted with Et2O (2×100 ml), washed with H2O, dried and essiccated in vacuo to leave 9.06 g of a white solid (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964679B2
Source datasetuspto-grants-2011_06
ORD IDord-9d421b647e2442d0926be3f11229ff3c
Source noteuspto-grants-2011_06