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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189495Generated: October 29, 2026

N-bromobutanimide → HCID 58296104, compound

https://huagongshe.com/reaction/2189495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-(4-(trifluoromethoxy)phenyl)acetateHCID 67219206—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 58296104HCID 58296104103.2%

Reaction Steps

A mixture of ethyl 2-(4-(trifluoromethoxy)phenyl)acetate (1.99 g, 8.00 mmol), N-bromosuccinimide (NBS) (1.57 g, 8.80 mmol) and 2,2′-azobis(2-methylpropionitrile) (AIBN) (66 mg, 0.400 mmol) in carbon tetrachloride (10 ml) was heated under reflux for 5 hours. The reaction mixture was concentrated in vacuo, diluted with diethyl ether (200 ml), washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo to give ethyl 2-bromo-2-(4-(trifluoromethoxy)phenyl)acetate (65) (2.70 g, quantitative yield) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324249B2
Source datasetuspto-grants-2012_12
ORD IDord-9892a53e21694c90831b0c320a44b269
Source noteuspto-grants-2012_12