Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458069Generated: October 27, 2026

1-Chloro-2,2-dimethylpropane → 2-(2,2-Dimethylpropyl)-n-ethyl-6-fluorobenzamide

https://huagongshe.com/reaction/1458069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2,2-dimethylpropaneHCID 12956—
ReactantSodium BicarbonateHCID 516892—
ReactantLithiumHCID 3028194—
ReactantOxazole, 2-(2,6-difluorophenyl)-4,5-dihydro-4,4-dimethyl-HCID 10987554—
SolventTetrahydrofuranHCID 8028—
Product2-(2,2-Dimethylpropyl)-n-ethyl-6-fluorobenzamideHCID 1862999527%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of p,p'-di-t-butyl biphenyl (5.559 g, 0.021 mol) and THF (100 mL) was stirred at 0° C. under an atmosphere of argon. Lithium wire (0.021 mol, 0.15 g) was added in small pieces and the mixture was allowed to stir at 0° C. for 24 h. The mixture was cooled to -78° C. and neopentyl chloride (2.0 g, 0.01875 mol) was added dropwise. The mixture was stirred at -78° C. for 1 h, and the compound of Example g (3.17 g, 0.015 mol) was added all at once. The mixture was continuously stirred for 4 h and 50 mL sat aq NaHCO3 was added. This mixture was extracted with three 50 mL portions of ethyl acetate. The combined extracts were washed twice with water, dried (MgSO4), and concentrated. The crude concentrate was purified by HPLC eluting with 1:4 ethyl acetate/hexanes. The oxazoline was as a clear oil in 27% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849723
Source datasetuspto-grants-1998_12
ORD IDord-735c8ac6febe4aeb9436eea5b782a350
Source noteuspto-grants-1998_12