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2-Methyl-4,5-trimethylene-4-isothiazolin-3-one → 1-Tertiarybutyldithio-2-methylaminocarbonylcyclopentene

HRID 486121
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반응식

HRID 486121 반응식
[CH3:1][N:2]1[S:7][C:6]2[CH2:8][CH2:9][CH2:10][C:5]=2[C:3]1=[O:4].[C:11]([SH:15])([CH3:14])([CH3:13])[CH3:12].[Na]>CO>[C:11]([S:15][S:7][C:6]1[CH2:8][CH2:9][CH2:10][C:5]=1[C:3]([NH:2][CH3:1])=[O:4])([CH3:14])([CH3:13])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1581902-Methyl-4,5-trimethylene-4-isothiazolin-3-oneHCID 450519182-Propanethiol, 2-methyl-, sodium salt

생성물 1

HCID 190975851-Tertiarybutyldithio-2-methylaminocarbonylcyclopentene

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

2-methyl-4,5-trimethylene-4-isothiazolin-3-one (0.78 parts) and sodium tertiary butyl mercaptan (0.56 parts) were stirred together in methanol (10 parts by volume) at 20° to 25° C. for 1 hour. The reactants were then drowned out into distilled water (100 parts by volume) and the disulphide reaction product (1 part) which separated was filtered and dried. The disulphide melted at 153°-5° C.

후처리

  1. distillationinto distilled water (100 parts by volume)
  2. customthe disulphide reaction product (1 part) which
  3. customseparated
  4. filtrationwas filtered
  5. customdried

출처 및 근거

ORD 기록
ord-5ca9379f5b2a4dffb5f34112ac1f9457
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05290810

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