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Cyclohexanesulfenyl chloride → HCID 11332618, 화합물

HRID 1076147
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HRID 1076147 반응식
C1(SCl)C=CC=CC=1.[CH2:9]([S:19][Cl:20])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]CCC.ClC(SCl)=CCl.C1C2C(=CC=CC=2)C=CC=1SCl.C1(SCl)CCCCC1>>[C:10]1([CH2:9][S:19][Cl:20])[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1
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참가 물질

6

반응물 5

HCID 87312Cyclohexanesulfenyl chlorideHCID 11008040Benzenesulfenyl chlorideHCID 124820622-Naphthalenesulfenyl chlorideHCID 21983338HCID 21983338, 화합물HCID 54122024HCID 54122024, 화합물

생성물 1

HCID 11332618HCID 11332618, 화합물

실험 절차

Similarly, repeating the above procedure but replacing the benzenesulfenyl chloride as used therein with an equal molar proportion of each of decanesulfenyl chloride (prepared by chlorination of decanedisulfide according to the method of Douglass, supra.), 1,2-dichlorovinylsulfenyl chloride, 2-naphthalenesulfenyl chloride, cyclohexanesulfenyl chloride (prepared by chlorination of cyclohexanedisulfide, according to the method of Douglass, supra.) and α-toluenesulfenyl chloride, respectively, there is obtained:

출처 및 근거

ORD 기록
ord-1d9f9f628582457596cd279bbb1dcb94
출처 데이터셋
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03954997

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