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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048114Generated: November 2, 2026

N-bromobutanimide → Methyl 6-bromo-7-fluoro-chromane-4-carboxylate

https://huagongshe.com/reaction/1048114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactantmethyl 7-fluoro-3,4-dihydro-2H-chromene-4-carboxylateHCID 67080260—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 6-bromo-7-fluoro-chromane-4-carboxylateHCID 4692918989.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

Methyl 7-fluoro-3,4-dihydro-2H-chromene-4-carboxylate (336 mg, 1.60 mmol) was diluted with DMF (5 mL) followed by the addition of N-bromosuccinimide (313 mg, 1.76 mmol). The reaction was heated at 50° C. and stirred for 2.5 hours. The reaction was cooled, diluted with ethyl acetate and washed with water, saturated sodium bicarbonate, water, and brine. The organic layer was dried over MgSO4, filtered and concentrated. The material was purified using a Biotage 40M cartridge, gradient 5% ethyl acetate/hexane to 50% to yield the title compound (415 mg, 89.8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569522B2
Source datasetuspto-grants-2013_10
ORD IDord-34a717e6ce224954b1be79a88f6e4143
Source noteuspto-grants-2013_10