Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220256Generated: October 26, 2026

N-(Diphenylmethylene)glycine tert-butyl ester → (2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoate

https://huagongshe.com/reaction/2220256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(Diphenylmethylene)glycine tert-butyl esterHCID 688171—
Reactant2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
ReactantO-Allyl-N-(9-anthracenylmethyl)cinchonidinium bromideHCID 10886583—
Reactant5-(Bromomethyl)-2-o-tolylpyridine hydrobromideHCID 67243566—
SolventDichloromethaneHCID 6344—
Product(2S)-tert-butyl 2-(diphenylmethyleneamino)-3-(6-o-tolylpyridin-3-yl)propanoateHCID 86609629100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred mixture of 800 mg (2.33 mmol) of 5-(bromomethyl)-2-o-tolylpyridine hydrobromide, 689 mg (2.33 mmol, 1.0 equivalent) of tert-butyl 2-(diphenylmethyleneamino)acetate and 141 mg (0.233 mmol, 0.1 equivalent) of O-allyl-N-(9-anthracenylmethyl)cinchonidinium bromide in 14 mL of dichloromethane at −78° C. under argon was added 1.687 mL (5.83 mmol, 2.5 eq) of 2-t-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine over 5 min. The reaction mixture was stirred at −78° C. for 10 h and then allowed to warm to room temperature in situ. The mixture was directly purified by silica gel chromatography using ethyl acetate/dichloro-methane (1:4) as eluant (5×10 cm column), to give tan oil, 1.10 g, 100% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417028B2
Source datasetuspto-grants-2008_08
ORD IDord-2f2c7abd700541a3be7adfe2c51eb938
Source noteuspto-grants-2008_08