Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348235Generated: 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/348235

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 numberUS07176235B2
Source datasetuspto-grants-2007_02
ORD IDord-c2dea00e9c53444ba8aa14cf3a136fbe
Source noteuspto-grants-2007_02