Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888412Generated: November 1, 2026

Diisopropylamine → Tert-butyl 5-(2,2-difluoro-1-hydroxyethyl)-2',4'-difluorobiphenyl-3-carboxylate

https://huagongshe.com/reaction/888412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
ReactantTrisodium 3,3',3''-phosphinetriyltris(benzene-1-sulphonate)HCID 6099338—
ReactantTert-butyl 3-bromo-5-(2,2-difluoro-1-hydroxyethyl)benzoateHCID 68501370—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductTert-butyl 5-(2,2-difluoro-1-hydroxyethyl)-2',4'-difluorobiphenyl-3-carboxylateHCID 6850033193.6%

Reaction Steps

To a solution of tert-butyl 3-bromo-5-(2,2-difluoro-1-hydroxyethyl)benzoate (1.0 g, 2.97 mmol) in N,N-dimethylformamide (11.9 mL) and water (2.97 mL) was added (2,4-difluorophenyl)boronic acid (0.61 g, 3.86 mmol), palladium(II) acetate (67 mg, 0.3 mmol), 3,3′3″-phosphinidynetris(benzenesulfonic acid)trisodium salt (0.51 g, 0.89 mmol) and diisopropylamine (1.27 mL, 8.9 mmol). The mixture was stirred at ambient temperature. After 1 h, brine was added and mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→60% hexanes/ethyl acetate) gave the title compound (1.03 g). MS 315.0 (M-t-butyl group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-7f6c911bbcf449bda699d8835a279541
Source noteuspto-grants-2012_08