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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021085Generated: October 31, 2026

3-Bromophenol → HCID 7663500, compound

https://huagongshe.com/reaction/1021085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
ReactantTriphenylphosphineHCID 11776—
ReactantN-(2-Hydroxyethyl)phthalimideHCID 77499—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventTetrahydrofuranHCID 8028—
ProductHCID 7663500HCID 7663500—

Reaction Steps

To an ice cold solution of 3-bromophenol (14) (2.0 g, 11.56 mmol), N-(2-hydroxyethyl)phthalimide (2.21 g, 11.6 mmol) and triphenyl phosphine (3.03 g, 11.6 mmol) in anhydrous THF (25 mL) was added diethyl azodicarboxylate (2.57 g, 12.7 mmol) slowly. The reaction mixture was allowed to warm to room temperature and stirred overnight. After concentration under reduced pressure, 50% EtOAc-hexanes (100 mL) was added and the mixture was warmed to 60° C. After cooling to room temperature, the solids were removed by filtration and the filtrate was concentrated under reduced pressure. Purification by flash chromatography (10% EtOAc-hexanes) gave bromide 17 as a white solid. Yield (1.92 g, 48%): 1H NMR (400 MHz, DMSO-d6) δ 7.82-7.88 (m, 4H), 7.19 (t, J=8.4 Hz, 1H), 7.06-7.09 (m, 2H), 6.87-6.90 (m, 1H), 4.22 (t, J=5.6 Hz, 2H), 3.93 (t, J=5.6 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716529B2
Source datasetuspto-grants-2014_05
ORD IDord-7e6c0a871ff04361b4e75dd6648616dd
Source noteuspto-grants-2014_05