HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377187Generated: October 25, 2026
Benzyl Alcohol → HCID 178503023, compound
https://huagongshe.com/reaction/377187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dichloromethylphosphite | HCID 18403142 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178503023 | HCID 178503023 | 50% |
Reaction Steps
Dichloromethylphosphite (10.0 g, 77 mmol) in 80 mL of dry diethyl ether was cooled to -20° C. under an atmosphere of nitrogen. A solution of benzyl alcohol (23 g, 213 mmol) and triethylamine (10.2 g, 100 mmol) in 40 mL of diethyl ether was added dropwise over 1 hour while maintaining an internal temperature range of 0° C. to 10° C. Once addition was complete the mixture was warmed to room temperature and stirred overnight. The mixture was filtered and the solid cake washed with 200 mL of diethyl ether. The organics were combined and evaporated under reduced pressure to give 25 g of a clear and colorless liquid. The liquid was purified by flash chromatography and eluted with a 1:1 hexane/ethyl acetate to ethyl acetate gradient. The desired fractions were collected and evaporated to give methyl O-benzylphosphinic acid (1, R=CH3,R1=CH2Ph, 6.5 g, 50%) as a clear and colorless oil. Rf 0.1 (1:1, Hexane/EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06025345 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-086154febfad4b4e91422e0a26a4a883 |
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| Source note | uspto-grants-2000_02 |
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