Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279743Generated: November 1, 2026

4-Chlorobutyryl chloride → HCID 15512391, compound

https://huagongshe.com/reaction/1279743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobutyryl chlorideHCID 78370—
Reactant2-[2-(4-Bromophenyl)propan-2-yl]-4,4-dimethyl-4,5-dihydro-1,3-oxazoleHCID 15512390—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15512391HCID 15512391—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 4-bromo-α,α-dimethyl-α-(4,4-dimethyloxazolin-2-yl)toluene (10.0 g. 0.0338 mole), prepared in accordance with Example 2, in 400 mL THF is cooled to −78° C., n-butyllithium (16 mL, 0.042 mole) is added via syringe, and the mixture is stirred at −78° C. for 30 minutes. While keeping the temperature below −75° C., 4-chlorobutyryl chloride (14.4 g, 0.102 mole) in 30 mL THF is added dropwise, and the mixture is stirred at −78° C. for 30 minutes. The mixture is allowed to warm to −15° C. and is quenched with water. The product is extracted with methylene chloride, washed with saturated NaCl solution, dried over Na2SO4, and concentrated. The residue is cooled to 0° C., treated with minimal acetonitrile, and filtered to afford 4-(4-chloro-1-oxobutyl)-α,α-dimethyl-α-(4,4-dimethyloxazolin-2-yl)toluene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448406B1
Source datasetuspto-grants-2002_09
ORD IDord-13a08f4c86444e6fa76b032b0821441f
Source noteuspto-grants-2002_09