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Dibromomethane → 2-Furfurylimino-1,3-dithietane

HRID 1973575
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HRID 1973575 반응식
[CH2:1]([NH:7][C:8](=[S:10])[S-:9])[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1.[CH2:11]([NH+](CC)CC)C.C(Br)Br.C(N(CC)CC)C.S1CCS1>CN(C)C=O>[CH2:1]([N:7]=[C:8]1[S:9][CH2:11][S:10]1)[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3024DibromomethaneHCID 8471TriethylamineHCID 123092831,2-DithietaneHCID 21453310Triethylammonium furfuryldithiocarbamate

생성물 1

HCID 214532962-Furfurylimino-1,3-dithietane

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

A mixture of 13.7 g. of triethylammonium furfuryldithiocarbamate, 10.5 ml. of methylene bromide, and 7.0 ml. of triethylamine in 100 ml. of dimethylformamide was stirred for several hours and then poured into ice-water. The oily product was partitioned into ether and the ether mixture was extracted with 3N hydrochloric acid. After extracting the acidic solution with methylene chloride, it was made basic with potassium hydroxide solution and re-extracted with methylene chloride. The methylene chloride mixture, after water washing, drying, and concentrating in vacuo afforded 4.9 g. of the desired dithietane as a yellow oil.

후처리

  1. additionA mixture of 13.7 g
  2. customThe oily product was partitioned into ether
  3. extractionthe ether mixture was extracted with 3N hydrochloric acid
  4. extractionAfter extracting the acidic solution with methylene chloride, it
  5. extractionre-extracted with methylene chloride
  6. dry with materialThe methylene chloride mixture, after water washing, drying
  7. concentrationconcentrating in vacuo
  8. customafforded 4.9 g

출처 및 근거

ORD 기록
ord-cb184dfcc68f43e7838d7b7ada97fbf4
출처 데이터셋
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03997668

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