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HRID 1707310作成日:2026年10月25日

Water → 20-{3-[N-(4-methylhexahydrophthalimido)amino]-3-oxopropyl}-2,2,4,4-tetramethyl-7-oxa-3,20-diazadispiro[5.1.11.2]heneicosane-21-one

https://huagongshe.com/reaction/1707310

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PentaneHCID 8003—
反応物Hexahydro-4-methylphthalic anhydrideHCID 86876—
反応物20-(3-Hydrazino-3-oxopropyl)-2,2,4,4-tetramethyl-7-oxa-3,20-diazadispiro[5.1.11.2]heneicosane-21-oneHCID 18963138—
溶媒O-XyleneHCID 7237—
生成物20-{3-[N-(4-methylhexahydrophthalimido)amino]-3-oxopropyl}-2,2,4,4-tetramethyl-7-oxa-3,20-diazadispiro[5.1.11.2]heneicosane-21-oneHCID 18963141—

反応手順

The hydrazide of Example 1, 13.5 g (0.03 mole), was added to 225 ml xylene at 75° C. Added dropwise to this was 4-methylhexahydrophthalic anhydride, 5.1 g (0.03 mole) in 25 ml xylene. The apparatus was fitted with a Dean Stark water separation assembly and the reaction mixture was heated to reflux for 4 hours with azeotropic removal of water as it formed. The xylenes were stripped using aspirator vacuum and the residual sticky solid was slurried with 300 ml pentane. The solid was filtered and dried for 2 hours on the filter funnel. The white solid product weighed 11.7 g and had a melting range of 210°-212° C. The infrared spectrum (mull) showed two carbonyl bands at 1690 and 1730 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05352719
出典データセットuspto-grants-1994_10
ORD IDord-1ce6e273f96b447ca991dee7f0f7384c
出典メモuspto-grants-1994_10