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HRID 579545作成日:2026年10月26日

Tetrahydrofuran → 1,1-Dimethylethyl 2-[(diphenylmethylene)amino]-5-hexenoate

https://huagongshe.com/reaction/579545

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Homoallyl bromideHCID 21241—
反応物N-(Diphenylmethylene)glycine tert-butyl esterHCID 688171—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒Diethyl EtherHCID 3283—
生成物1,1-Dimethylethyl 2-[(diphenylmethylene)amino]-5-hexenoateHCID 1606697494%

反応手順

While under an atmosphere of argon, a solution of N-(diphenylmethylene)glycine tert-butyl ester (6.30 g, 21.33 mmol) and 4-bromo-butene (3.45 g, 25.56 mmol) in freshly distilled THF (50 mL) was cooled to −78° C. and treated with sodium bis(trimethylsilyl)amide (23.4 mL, 1.0 M in THF). Once the addition was complete, the reaction was warmed to room temperature and stirred for 16 h, cooled to 0° C., diluted with ethyl ether and washed successively with saturated aqueous NaHCO3 and saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. Rapid purification by MPLC (1-25% ethyl acetate in heptane over 8 CV) gave product tert-butyl 2-(diphenylmethyleneamino)hex-5-enoate as a colorless oil (7.00 g, 94%). Rf 0.50 (30% ethyl acetate in heptane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040703B2
出典データセットuspto-grants-2015_05
ORD IDord-3f97ef19311e49cc876029c1e88f0688
出典メモuspto-grants-2015_05