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HRID 1689208作成日:2026年10月27日

Triethylamine → 2-Methylpentane

https://huagongshe.com/reaction/1689208

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5-Methylthiophene-2-carboxylic acidHCID 74713—
反応物Propylphosphonic anhydrideHCID 111923—
反応物Tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochlorideHCID 66964240—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-MethylpentaneHCID 7892—
生成物Tert-butyl 4-(5-methylthiophene-2-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylateHCID 57989101—

反応手順

1-Propanephosphonic acid cyclic anhydride (1.57M solution in THF, 0.64 mL) was added to a solution of tert-butyl 1-oxa-4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride (WuXi PharmaTech) (0.26 g), 5-methylthiophene-2-carboxylic acid (0.142 g) and triethylamine (0.84 mL) in DMF (8 mL) and the resulting mixture stirred for 16 h. The reaction mixture was poured into water (100 mL) and extracted with ethyl acetate (3×200 mL). The combined organic solutions were washed with water (2×100 mL) and brine (100 mL), then dried over magnesium sulphate, filtered and evaporated in vacuo. Purification was by silica gel chromatography eluting with ethyl acetate:isohexane, 1:1 to give the subtitled compound as a clear oil. Yield 0.32 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08148373B2
出典データセットuspto-grants-2012_04
ORD IDord-2bea720a39d74bf59b258f8b62f8270c
出典メモuspto-grants-2012_04