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HRID 29711作成日:2026年10月27日

Acetyl chloride → Methyl 4-(2-aminoethoxy)benzoate hydrochloride

https://huagongshe.com/reaction/29711

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物MethylparabenHCID 7456—
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物tert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-(2-aminoethoxy)benzoate hydrochlorideHCID 5098856893.5%

反応条件

温度2.5 °C

反応手順

(2-Hydroxyethyl)carbamic acid tert-butyl ester (152.0 g, 0.942 mol) and 4-hydroxybenzoic acid methyl ester (174.0 g, 1.12 mol) were dissolved in tetrahydrofuran (2000 ml) and cooled to 0-5° C. Triphenylphosphine (292.8 g 1.116 mol) was added to the cooled mixture. A solution of diisopropyl azodicarboxylate (246.0 g, 1.218 mol) in tetrahydrofuran (400 ml) was added dropwise over a period of one to two hours keeping the reaction temperature below 10° C. After addition, the reaction was allowed to warm slowly to ambient temperature and stirred overnight. After completion of reaction, solvent was distilled under reduced pressure and the resulting oil was dissolved in ethanol (500 ml) and ethyl acetate (2000 ml). Acetyl Chloride (222.0 g, 2.826 mol) was added drop wise over fifteen minutes with the temperature allowed to rise to 40° C. The resulting suspension was stirred at 40° C. until completion of reaction. After completion of reaction, the resulting crystals were filtered on a coarse frit and washed with ethyl Acetate (300 mL). The material is dried in vacuo to give of 4-(2-aminoethoxy)benzoic acid methyl ester hydrochloride (204.1 g) as a white crystalline solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420089B2
出典データセットuspto-grants-2008_09
ORD IDord-1e38f5e010734ba593a554c9bb24cb2d
出典メモuspto-grants-2008_09