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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357396Generated: October 26, 2026

Ammonium Chloride → (4R,5S,6S)-1,1-diisopropoxy-5-hydroxy-2,2,4,6-tetramethyl-8-nonen-3-one

https://huagongshe.com/reaction/1357396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
Reactant(2S)-2-methyl-4-pentenalHCID 10176097—
Reactant1,1-Diisopropoxy-2,2-dimethyl-3-pentanoneHCID 11322179—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(4R,5S,6S)-1,1-diisopropoxy-5-hydroxy-2,2,4,6-tetramethyl-8-nonen-3-oneHCID 11198250—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 1,1-diisopropoxy-2,2,-dimethyl-3-pentanone (3.29 g) in 15 mL of THF is added slowly to a solution of lithium diisopropylamide (15.7 mmol) in 20 mL of THF cooled to −78° C., the mixture is stirred for 30 minutes, warmed to −40° C. and stirred for 30 minutes, then recooled to −78° C. A solution of (2S)-2-methyl-4-pentenal (16.36 mmol) in 2 mL of CH2Cl2 is added and the mixture is stirred for 1 hour at −78° C. Saturated aq. NH4Cl is added and the mixture is warmed to ambient temperature and extracted with ethyl acetate. The extract is dried over Na2SO4, filtered, and evaporated. The residue is purified by silica gel chromatography (2% ethyl acetate/hexanes) to separate the two diastereomeric products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589968B2
Source datasetuspto-grants-2003_07
ORD IDord-20224d720c7849919f5323e36967a0a8
Source noteuspto-grants-2003_07