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HRID 473548作成日:2026年10月25日
[(S)-1-(Methoxy-methyl-carbamoyl)-2-methyl-propyl]carbamic acid benzyl ester → benzyl [(1S)-1-formyl-2-methylpropyl]carbamate
https://huagongshe.com/reaction/473548
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | [(S)-1-(Methoxy-methyl-carbamoyl)-2-methyl-propyl]carbamic acid benzyl ester | HCID 10469699 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | benzyl [(1S)-1-formyl-2-methylpropyl]carbamate | HCID 11009915 | 99.8% |
反応手順
To a solution of [(S)-1-(Methoxy-methyl-carbamoyl)-2-methyl-propyl]-carbamic acid benzyl ester (8) (33 g, 112 mmol) in dry THF (300 mL) at −30 to −40° C. was added LiAlH4 (4.3 g, 113 mmol) portion wise over a period of 45 min. The reaction mixture was warmed to 0° C. and stirred at this temperature for 2 h. The reaction mixture was quenched with 1 M KHSO4 (330 mL) at 0° C. then 10% w/v Rochelle's salt (aq) (330 mL) was added and the mixture stirred for 20 minutes, then extracted with EtOAc (2×700 mL). The combined organic phases were washed with 10% w/v Rochelle's salt (aq) (330 mL) and brine (450 mL), dried over MgSO4, filtered and concentrated under vacuum to obtain the desired aldehyde as a clear oil (26.3 g) (AnalpH2_MeOH—4 min) Rt 2.59 min; m/z 236 (MH)+. (This was used without further purification in the next step.)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08637453B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-d28217c9700945d6b1f9610f03e86d4c |
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| 出典メモ | uspto-grants-2014_01 |
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