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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204041Generated: October 30, 2026

4-Bromo-1-chloro-2-(4-ethoxy-benzyl)-benzene → HCID 66884302, compound

https://huagongshe.com/reaction/2204041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1-chloro-2-(4-ethoxy-benzyl)-benzeneHCID 9996449—
ReactantHCID 59431063HCID 59431063—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66884302HCID 6688430230%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-bromo-1-chloro-2-(4-ethoxy-benzyl)-benzene from step C (3.6 g, 11.1 mmol) in THF (60 ml) under N2 at −78° C. was added dropwise BuLi (2.5 M in hexanes, 4.4 ml, 11.1 mmol). After 30 minutes, aldehyde from step B (2.4 g, 64% clean, 5.1 mmol) in THF (20 ml) was added dropwise, and the reaction was stirred for 30 min at −78° C., allowed to warm to room temperature and stirred for 60 minutes, quenched with sat. aq. NH4Cl, diluted with Et2O, and washed with H2O and brine. The combined aqueous washes were back extracted with Et2O, which was washed by the same sequence. The combined organic extracts were dried over MgSO4, filtered, and concentrated under vacuum. The residue was purified by flash chromatography (120 g SiO2, 0-20% EtOAc:Hexanes, 75 minutes, 85 ml/min) to give clean (S)-[(3aS,5S,6R,6aS)-6-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-methanol (0.84 g, 1.5 mmol, 30%) plus the C5 epimer (0.83 g) and some mixed fractions (0.51 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365602B2
Source datasetuspto-grants-2016_06
ORD IDord-0dd805ae569440138f02ab2225f4e603
Source noteuspto-grants-2016_06