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HRID 451762作成日:2026年10月27日

Ethanaminium, N,N,N-triethyl-, fluoride (1:1) → (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate

https://huagongshe.com/reaction/451762

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanaminium, N,N,N-triethyl-, fluoride (1:1)HCID 69582—
反応物(S)-tert-butyl 1-(2-(trimethylsilyl)ethoxycarbonylamino)-3-cyclohexylpropan-2-ylcarbamateHCID 59382914—
溶媒AcetonitrileHCID 6342—
生成物(S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamateHCID 1098890485.9%

反応条件

温度60 °C

反応手順

To a stirred solution of (S)-tert-butyl 1-(2-(trimethylsilyl)ethoxycarbonylamino)-3-cyclohexylpropan-2-ylcarbamate (6.55 g, 15.4 mmol) in MeCN (100 mL) was added Et4NF (7.5 g, 50 mmol). The mixture was stirred overnight at rt and at 60° C. for 7 h. The mixture was concentrated and the oily residue was taken up in EtOAc (175 mL). The mixture was washed with water (2×50 mL) and brine (50 mL) and dried over Na2SO4. Removal of the solvent afforded (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate (3.39 g, 80%) as a syrup.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08487108B2
出典データセットuspto-grants-2013_07
ORD IDord-18651ba18c464d10a01bba32b765863c
出典メモuspto-grants-2013_07