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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451513Generated: October 27, 2026

Ethylene Oxide → [1,1'-Biphenyl]-2-ethanol

https://huagongshe.com/reaction/1451513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
Reactant2-BromobiphenylHCID 16329—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product[1,1'-Biphenyl]-2-ethanolHCID 2205202149.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromobiphenyl (20.0 g, 86 mmol) in THF (85 ml) was dropwise added to a refluxing suspension of magnesium (2.1 g, 86 mmol) in THF (15 ml). The reaction mixture was refluxed for 18 h and an extra batch of 2-bromobiphenyl (2.0 g, 8.6 mmol) was added. The reaction mixture was refluxed for 2 h and cooled to 0° C. on an icebath. Ethyleneoxide (14.0 g, 0.32 mol) was was added. The reaction mixture was refluxed for 18 h, cooled to 0° C. and a saturated solution of ammonium chloride (100 ml) was dropwise added at this temperature. The reaction mixture was diluted with diethyl ether (100 ml) and concentrated hydrochloric acid was added until pH 2. The organic phase was separated, dried (MgSO4) and concentrated in vacuo. The residue was submitted to column chromatography on silica gel (800 ml) using heptane and ethyl acetate (7:3) as eluent to give 8.5 g of 2-(biphenyl-2-yl)ethanol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604242
Source datasetuspto-grants-1997_02
ORD IDord-3dc860761bbc47edbfcf113b2754556b
Source noteuspto-grants-1997_02