Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427373Generated: November 1, 2026

(1,1'-Biphenyl)-2-ol → HCID 4539764, compound

https://huagongshe.com/reaction/427373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,1'-Biphenyl)-2-olHCID 7017—
ReactantEthyl bromoacetateHCID 7748—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventAcetonitrileHCID 6342—
ProductHCID 4539764HCID 4539764—

Reaction Steps

In 10 ml of acetonitrile, 1.0 g of o-phenylphenol and 1.29 ml of ethyl bromoacetate were added in the presence of 1.76 ml of 1,8-diazabicyclo[5.4.0]-7-undecene (DBU) and the resultant mixture was refluxed for 8 hr. The reaction mixture was treated similarly to that in Example 28 (Process 2) to give 1.46 g of ethyl o-phenylphenoxyacetate. The ester was dissolved in 30 ml of ethanol, mixed with 10.8 ml of 1N-NaOH aqueous solution and stirred for 12 hr. The reaction mixture was evaporated under reduced pressure, acidified by the addition of 1N-HCl and extracted with ethyl acetate. The extract was washed with saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure and o-phenylphenoxyacetic acid was crystallized as DCHA salt from ether with the yield of 1.59 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313094B1
Source datasetuspto-grants-2001_11
ORD IDord-937bbb3415484d4d88d8cd6b860f1c26
Source noteuspto-grants-2001_11