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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486049Generated: October 28, 2026

Acetone → HCID 19097396, compound

https://huagongshe.com/reaction/486049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 19097382HCID 19097382—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 19097396HCID 1909739699%

Reaction Steps

A mixture of 2,3,4-trimethyl-3-piperidinepropanol (13.0 g, 70 mmol), acetone (400 mL), methanol (300 mL), sodium cyanoborohydride (4.4 g, 70 mmol), 3A molecular sieves (30 g) and acetic acid (4.0 mL, 70 mmol) was stirred under a nitrogen atmosphere for 2 hours. The pH was readjusted to a pH of 5 by the addition of 1.5 mL of additional acetic acid and the reaction mixture was stirred for 24 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was dissolved in water (200 mL) and acetone (20 mL) and was acidified with concentrated hydrochloric acid. The mixture was basified with 10% NAOH and extracted with ether (4×300 mL) . The ether extracts were combined, washed with brine and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by a Kugelrohr distillation at 0.1 mm Hg and 100-110° C. to afford 15.7 g (99%) of 2,3. 4-trimethyl-l- (1-methylethyl)-3-piperidinepropanol as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290789
Source datasetuspto-grants-1994_03
ORD IDord-dcfa93949724403793cd9c7e296c2c53
Source noteuspto-grants-1994_03