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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
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-ylcarbamate | HCID 59382914 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (S)-tert-butyl 1-amino-3-cyclohexylpropan-2-ylcarbamate | HCID 10988904 | 85.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08487108B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-18651ba18c464d10a01bba32b765863c |
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| 出典メモ | uspto-grants-2013_07 |
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