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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574235Generated: October 29, 2026

Benzyl Bromide → HCID 86729607, compound

https://huagongshe.com/reaction/574235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 10977790HCID 10977790—
SolventDimethylformamideHCID 6228—
ProductHCID 86729607HCID 86729607—

Reaction Conditions

Temperature0 °C

Reaction Steps

A cooled (0° C.) solution of benzyl 3,3,3-trifluoro-2-hydroxy-2-methylpropanoate (Int. D1) (100 mg, 0.403 mmol) in DMF (4 ml) was treated with sodium hydride (16.11 mg, 0.403 mmol) followed by benzyl bromide (0.048 ml, 0.403 mmol) and stirred at 0° C. for 2 h. The reaction mixture was allowed to warm to room temperature and stirring continued for a further 3 hrs. The reaction mixture was partitioned between EtOAc and 0.1M HCl solution. The organic phase was washed with saturated brine, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034879B2
Source datasetuspto-grants-2015_05
ORD IDord-fc98e88aa8084d7caad1b7f51fc37ec3
Source noteuspto-grants-2015_05