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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003174Generated: October 30, 2026

Benzyl Alcohol → HCID 18403062, compound

https://huagongshe.com/reaction/1003174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantHCID 178520628HCID 178520628—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18403062HCID 1840306248.5%

Reaction Steps

To a solution of 2,4-di-(benzyloxycarbonyl)butyl phosphinic acid (6) (19.3 g, 49.4 mmol) in tetrahydrofuran was added benzyl alcohol (5.3 g, 49.3 mmol) and dimethylamino in tetrahydrofuran was added benzyl alcohol (5.3 g, 49.3 mmol) and dimethylamino pyridine (0.5 g). Dicylcohexylcarbodiimide (DCC, 12 g, 58 mmol) was added and a white precipitate formed. After 30 minutes the white suspension was filtered and the filtrate evaporated under reduced pressure. The clear and colorless oil was purified by flash chromatography and eluted with 1:1 Hex./EtOAc to give 2,4-di(benzyloxycarbonyl)butylbenzylphosphinic acid (7) (11.5 g, 47%) as a clear and colorless oil. Rf. 0.16 (1:1 Hex./EtOAc); 1H NMR (CDCl3): 7.3 ppm (m,15H), 7.2 ppm (d,1H), 5.0 ppm (m,6H), 2.9 ppm (m,1H), 2.2 ppm (m,3H), 1.9 ppm (m,3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046180
Source datasetuspto-grants-2000_04
ORD IDord-2078fa06430844b39575cbffb1cba125
Source noteuspto-grants-2000_04