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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579525Generated: October 25, 2026

Benzoyl chloride → 2-(Benzhydrylidene-amino)-2-benzoyl-hex-5-enoic acid tert-butyl ester

https://huagongshe.com/reaction/579525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant1,1-Dimethylethyl 2-[(diphenylmethylene)amino]-5-hexenoateHCID 16066974—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzhydrylidene-amino)-2-benzoyl-hex-5-enoic acid tert-butyl esterHCID 86663724100%

Reaction Steps

A solution of 2-(benzhydrylidene-amino)-hex-5-enoic acid tert-butyl ester (350 mg, 1 mmol) in THF (5 mL, 0.2 M) was cooled to −78° C. and treated with sodium bis(trimethylsilyl)amide (2.2 mL, 1.0 M, 2.2 equiv) drop wise over 5 min and stirred for 30 min. After adding benzoyl chloride (140 μl, 1.2 mmol, 1.2 eq), the reaction mixture was warmed up to room temperature and stirred for an additional 1.5 h. The solution was cooled to 0° C. and quenched with water (5 mL). The resulting solution was diluted with ethyl acetate and washed successively with water and saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. Purification by MPLC (1-40% ethyl acetate in heptane gave 2-(benzhydrylidene-amino)-2-benzoyl-hex-5-enoic acid tert-butyl ester (477 mg, 1 mmol, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040703B2
Source datasetuspto-grants-2015_05
ORD IDord-b217d9585daf41bb84cf645283863799
Source noteuspto-grants-2015_05