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Dimethyl Sulfoxide → Dilauryl disulfide

HRID 1075996
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반응식

HRID 1075996 반응식
C[S:2]([CH3:4])=O.[CH2:5]([SH:17])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>Cl.II>[CH2:5]([S:17][S:2][CH2:4][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH3:5])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 679Dimethyl SulfoxideHCID 81951-Dodecanethiol

생성물 1

HCID 151040Dilauryl disulfide수율 90%

시약·촉매·용매 2

HCID 313Hydrochloric Acid촉매HCID 807Iodine촉매

반응 조건

온도
60 °C

실험 절차

A mixture of 9 ml of DMSO (127 mmole), 12 ml of 1-dodecanethiol (50 mmole), 0.1 ml of 37 percent hydrochloric acid (1.2 mmole), and 10.8 mg of iodine (0.085 mmole as HI) was heated by a bath, while stirring magnetically, at about 60°C. After one and a fourth hours, the lower phase became amber colored. The mixture was cooled with stirring to produce fine crystals. These were filtered off and rinsed with DMSO. Recrystallization from acetone gave 9.02 g of didodecyl disulfide (90 percent of theory). Mp, 33°-5°C. (reported, 33°-4°C.).

후처리

  1. temperaturewas heated by a bath
  2. temperatureThe mixture was cooled
  3. stirringwith stirring
  4. customto produce fine crystals
  5. filtrationThese were filtered off
  6. washrinsed with DMSO
  7. customRecrystallization from acetone

출처 및 근거

ORD 기록
ord-600f13a40cc94b9597245da9428a9f42
출처 데이터셋
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03954800

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