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Triethylamine → N-(pentafluorobenzene-sulfonyl)methacrylamide

HRID 618959
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HRID 618959 반응식
[F:1][C:2]1[C:7]([S:8]([NH2:11])(=[O:10])=[O:9])=[C:6]([F:12])[C:5]([F:13])=[C:4]([F:14])[C:3]=1[F:15].C(N(CC)CC)C.[C:23](Cl)(=[O:27])[C:24]([CH3:26])=[CH2:25]>CN(C1C=CN=CC=1)C.CN(C)C=O>[F:1][C:2]1[C:7]([S:8]([NH:11][C:23](=[O:27])[C:24]([CH3:26])=[CH2:25])(=[O:10])=[O:9])=[C:6]([F:12])[C:5]([F:13])=[C:4]([F:14])[C:3]=1[F:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 13528Methacryloyl chlorideHCID 2063927Pentafluorobenzenesulfonamide

생성물 1

HCID 21845202N-(pentafluorobenzene-sulfonyl)methacrylamide수율 61.9%

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매HCID 6228
Dimethylformamide
용매

실험 절차

Using 24.7 g (0.1 mol) of pentafluorobenzene-sulfonamide, 1.2 g (0.01 mol) of 4-(N,N-dimethylamino)pyridine, 22.3 g (0.22 mol) of triethylamine, 13.5 g (0.12 mol) of methacryloyl chloride, and 100 ml of dimethylformamide, reaction was conducted in the same manner as in Synthesis Example 1. As a result, 19.5 g of N-(pentafluorobenzene-sulfonyl)methacrylamide was obtained (yield, 61.9%; light-yellow crystals; m.p., 133-133.5° C.).

후처리

  1. customwas conducted in the same manner as in Synthesis Example 1

출처 및 근거

ORD 기록
ord-f69ec77881bd410f9c5ce7ef5f0594a3
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05958646

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