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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468639Generated: October 29, 2026

Phosphorodichloridic acid, phenyl ester → HCID 86693901, compound

https://huagongshe.com/reaction/1468639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorodichloridic acid, phenyl esterHCID 13038—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57360154HCID 57360154—
SolventDichloromethaneHCID 6344—
ProductHCID 86693901HCID 86693901—

Reaction Steps

1-Butanol (1200 mL) was cooled to −20° C. and 50 mL of SOCl2 added with stirring followed by 50 g (33.67 mmol) of (S)-2-aminopropanoic acid. The solution was heated 24 hrs at reflux, most of the solvent stripped off, and the residue was dissolved in 800 mL of diethyl ether. The mixture was left for 1 hr at 0° C. to afford (S)-butyl 2-aminopropanoate hydrochloride (intermediate 11.47 g). Phenyl phosphorodichloridate (48.9 g, 232 mmol) and (S)-butyl 2-aminopropanoate hydrochloride (42 g, 232 mmol) were suspended in anhydrous CH2Cl2 (200 mL). N,N-diisopropylethylamine (59.9 g, 464 mmol) was added drop wise at −78° C., and after 4 hrs the reaction was concentrated. Diethylether (Et2O, 500 mL) was added and the resulting precipitate was filtered off and washed with dry Et2O (twice 100 mL). The filtrate was evaporated to dryness. (2S)-butyl 2-(chloro(phenoxy)phosphorylamino)propanoate (12) was stored as 0.5 M solution in THF at −18° C. until further reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006209B2
Source datasetuspto-grants-2015_04
ORD IDord-bfed9a8276ea457791cee6a45b696e2b
Source noteuspto-grants-2015_04