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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497543Generated: October 31, 2026

HCID 131734215, compound → HCID 84776658, compound

https://huagongshe.com/reaction/1497543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131734215HCID 131734215—
SolventHydrogen BromideHCID 260—
ProductHCID 84776658HCID 8477665836.5%

Reaction Steps

tert-Butyl 3 (2,6-difluoro-4-methoxyphenyl)propanoate (11.7 g) was suspended in 48% aqueous hydrogen bromide (200 mL), followed by stirring at 120 □ C for 16 hours. The reaction mixture was concentrated under reduced pressure, and then to the residue was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 3-(2,6-difluoro-4-hydroxyphenyl)propanoic acid (3.17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199927B2
Source datasetuspto-grants-2015_12
ORD IDord-5b71a232e49943eaba6b4f11bbb0bd97
Source noteuspto-grants-2015_12