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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100369Generated: November 1, 2026

Carbon Tetrachloride → Methyl 2-(4-(bis(benzyloxy)phosphoryloxy)phenyl)acetate

https://huagongshe.com/reaction/2100369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzeneacetic acid, 4-hydroxy-, methyl esterHCID 518900—
ReactantDibenzylphosphiteHCID 21904359—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-(4-(bis(benzyloxy)phosphoryloxy)phenyl)acetateHCID 5779905088.5%

Reaction Steps

To a solution of methyl 2-(4-hydroxyphenyl)acetate (1.89 g, 11.4 mmol) in acetonitrile (90 mL) at −10° C. was added CCl4 (5.5 mL, 57 mmol), DIPEA (4.16 mL, 23.9 mmol) and DMAP (139 mg, 1.14 mmol). After stirring for 10 mins, the mixture was added dibenzyl phosphite (3.7 mL, 16.5 mmol) slowly to keep the temperature below −10° C. The reaction was stirred at −10° C. for 1 h. The reaction was quenched with aqueous K2HPO4 (0.5 M) in acetonitrile (60 mL) and allowed to stirred at rt. The mixture was extracted by ethyl acetate (150 mL×3). The combined organic layers was washed with water and brine, dried over Na2SO4, filtered and concentrated under vacuum. The residue was subjected to ISCO (30-50% AcOEt/hexanes) to give the title compound (4.3 g, 88.5% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572795B2
Source datasetuspto-grants-2009_08
ORD IDord-e3e83edaa85f472b85c026b5b15a26ad
Source noteuspto-grants-2009_08