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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805255Generated: October 30, 2026

Benzophenone imine → HCID 86653294, compound

https://huagongshe.com/reaction/1805255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenone imineHCID 136809—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 67151671HCID 67151671—
SolventTolueneHCID 1140—
ProductHCID 86653294HCID 8665329482%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of (4S,5S)-4-[2-(4-bromo-phenyl)-ethyl]-2,2,5-trimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (3.13 g) in toluene (30 ml) were added diphenylmethanimine (1.71 g) and sodium tert-butoxide (1.06 g). The reaction mixture was degassed by bubbling argon through the mixture for several minutes. BINAP (489 mg) and Pd2(dba)3 (216 mg) were then added and the reaction mixture was stirred at 100° C. for 20 h. The reaction mixture was then cooled to room temperature, poured into EtOAc, and extracted with water. The organic layer was separated, dried over Na2SO4, and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, gradient: 0% to 30% EtOAc in hexane) to afford (4S,5S)-4-{2-[4-(benzhydrylidene-amino)-phenyl]-ethyl}-2,2,5-trimethyl-oxazolidine-3-carboxylic acid tert-butyl ester as a yellow oil (3.2 g, 82%). MS (ISP): 499.3 ([M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354441B2
Source datasetuspto-grants-2013_01
ORD IDord-218eb368d4a845c4b0283a1dc7605fce
Source noteuspto-grants-2013_01