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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505337Generated: October 29, 2026

Acetaldehyde → HCID 86608959, compound

https://huagongshe.com/reaction/505337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 15500645HCID 15500645—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86608959HCID 8660895958.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

At −78° C. under nitrogen 1.6 M butyllithium solution in hexane (13.8 ml, 20 mmol) were added dropwise to (2-Bromo-5-trifluoromethyl-phenyl)-carbamic acid tert-butyl ester (3.4 g, 10 mmol) in THF (60 ml). The reaction was stirred for 15 minutes at −78° C. and acetaldehyde (881 mg, 20 mmol) was added dropwise. After stirring for 15 minutes at −78° C. saturated aqueous ammonium chloride solution was added and the reaction was allowed to warm to room temperature. The reaction was diluted with water and extracted twice with diethyl ether. The combined organic layers were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and the solvent was evaporated to yield the crude product which was purified by column chromatography (heptane:ethyl acetate=7:3). The product was isolated as a yellow viscous oil (1.78 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781441B2
Source datasetuspto-grants-2010_08
ORD IDord-97dd83b13d664666ba4030548c98a175
Source noteuspto-grants-2010_08