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HRID 487457作成日:2026年10月25日

Water → 10-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-decanoic acid ethyl ester

https://huagongshe.com/reaction/487457

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物5-[8-(N-benzyloxycarbonylamino)oct-1-en-2-yl]-oxazoline-4-carboxylic acid ethyl esterHCID 14966608—
溶媒TetrahydrofuranHCID 8028—
生成物10-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-decanoic acid ethyl esterHCID 14966609—

反応手順

8.15 g (20.25 mmol) of 5-[8-(N-benzyloxycarbonylamino)oct-1-en-2-yl]-oxazoline-4-carboxylic acid ethyl ester are heated under reflux in 40 ml of tetrahydrofuran and 20 ml of water for 4 hours with stirring. The reaction mixture is concentrated to dryness by evaporation in vacuo at 45°, and the honey-like residue is concentrated by evaporation twice more after the addition of toluene. The crude product is dissolved in dichloromethane, dried with sodium sulfate, filtered and concentrated by evaporation. Drying under a high vacuum at room temperature yields 9.03 g of 10-(N-benzyloxycarbonylamino)-2-formylamino-3-hydroxy-4-methylene-decanoic acid ethyl ester in the form of a yellowish honey.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05294734
出典データセットuspto-grants-1994_03
ORD IDord-f9c6d02cc10e4456bedf8b9288604295
出典メモuspto-grants-1994_03