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Tetrahydrophthalic anhydride → 2-Octadecyl-4,7,3a,7a-tetrahydroisoindole-1,3-dione

HRID 566418
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인쇄 미리보기

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HRID 566418 반응식
[CH2:1]([NH2:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C:20]1(=O)[CH:28]2[CH:23]([CH2:24][CH:25]=[CH:26][CH2:27]2)[C:22](=[O:29])[O:21]1>>[CH2:1]([N:19]1[C:20](=[O:21])[CH:28]2[CH:23]([CH2:24][CH:25]=[CH:26][CH2:27]2)[C:22]1=[O:29])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
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참가 물질

3

반응물 2

HCID 6810Tetrahydrophthalic anhydrideHCID 15793Octadecylamine

생성물 1

HCID 212661442-Octadecyl-4,7,3a,7a-tetrahydroisoindole-1,3-dione수율 98.7%

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온도
110 °C

실험 절차

Octadecylamine (5.31 g) was added to 4,7,3a,7a-tetrahydroisobenzofuran-1,3-dione (3.00 g). After being stirred for 2 hours at 110° C., the reaction mixture was purified by silica gel column chromatography (silica gel 80 g, chloroform), thereby yielding the entitled compound (7.85 g) as yellow crystals.

후처리

  1. customthe reaction mixture was purified by silica gel column chromatography (silica gel 80 g, chloroform)

출처 및 근거

ORD 기록
ord-ad23ef1d4f0946fd99ee776370455660
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06174885B1

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