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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855285Generated: October 27, 2026

Water → HCID 86603039, compound

https://huagongshe.com/reaction/855285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
ReactantHCID 39072071HCID 39072071—
SolventDimethylformamideHCID 6228—
ProductHCID 86603039HCID 8660303973%

Reaction Steps

A solution of 224 mg of 2,2,2-trifluoro-N-[2-(4-methyl-thiazol-2-yl)-ethyl]-acetamide (0.94 mmol) in 4 ml DMF was added to a suspension of 45 mg of sodium hydride (60% in mineral oil) in 4 ml DMF at 0° C. After 30 min 0.173 ml 4-tert-butyl-benzylbromide were added and the reaction mixture was allowed to warm to rt. Stirring was continued for 3 h at ambient temperature, then water was added and the mixture was extracted with EtOAc. The organic layers were dried over magnesium sulfate, filtrated and the solvent was evaporated. Chromatography (silica gel; cyclohexane/EtOAc 4:1) yielded 265 mg (73%) of N-(4-tert-butyl-benzyl)-2,2,2-trifluoro-N-[2-(4-methyl-thiazol-2-yl)-ethyl]-acetamide as a light yellow liquid. 1H NMR (CDCl3, 300 MHz): δ 1.30 (s) and 1.31 (s, 9H), 2.42 (s, 3H), 3.23 (q, J=7 Hz, 2H), 3.70 (t, J=7 Hz) and 3.79 (t, J=7 Hz, 2H), 4.48(s) and 4.62 (s, 2H), 6.77 (m, 1H), 7.10 (d, J=8 Hz) and 7.17 (d, J=8 Hz, 2H), 7.36 (d, J=8 Hz) and 7.38 (d, J=8 Hz, 2H); MS (ISP) 385.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-e5f5193120b34494b1179071c78de6cc
Source noteuspto-grants-2007_08