戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 4529作成日:2026年10月24日

((p-(Benzyloxy)phenoxy)methyl)oxirane → 1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-benzyloxyphenoxy)propan-2-ol

https://huagongshe.com/ja/reaction/4529

反応式

関与物質

役割名称HCID仕込み量
反応物((p-(Benzyloxy)phenoxy)methyl)oxiraneHCID 119882—
反応物6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-oneHCID 13754414—
溶媒IsopropanolHCID 3776—
生成物1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-benzyloxyphenoxy)propan-2-olHCID 13754411—

反応手順

A solution of 15.4 g of benzyl [4-(2,3-epoxypropoxy)phenyl]ether and 17.0 g of 6-(2-benzylaminopropoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one in 100 ml of isopropanol is refluxed for 24 hours, filtered and concentrated by evaporation. Trituration of the residue with approximately 200 ml of ether results in crystallisation of 1-[N-[2-(2,3-dihydro-2,2-dimethyl-4-oxo-4H-1,3-benzoxazin-6-yloxy)-1-methylethyl]benzylamino]-3-(4-benzyloxyphenoxy)propan-2-ol having a melting point of 149°-160° (in which the enantiomer pair A is present in greater amount).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727067
出典データセットuspto-grants-1988_02
ORD IDord-75fb8b38e64d40b591e7fff45e062a05
出典メモuspto-grants-1988_02