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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzeneacetic acid, 4-hydroxy-, methyl ester | HCID 518900 | — |
| Reactant | Dibenzylphosphite | HCID 21904359 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-(4-(bis(benzyloxy)phosphoryloxy)phenyl)acetate | HCID 57799050 | 88.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572795B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-e3e83edaa85f472b85c026b5b15a26ad |
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| Source note | uspto-grants-2009_08 |
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