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Phosphorus oxychloride → 3-(2-Thienyl)-2-propenenitrile

HRID 596772
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HRID 596772 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]=[CH:7][C:8]([NH2:10])=O.S(S([O-])=O)([O-])(=O)=O.[Na+].[Na+].P(Cl)(Cl)(Cl)=O>O>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]=[CH:7][C:8]#[N:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24813Phosphorus oxychloride2회HCID 912113-(2-Thienyl)acrylamideHCID 656671Sodium Pyrosulfite

생성물 1

HCID 1111403-(2-Thienyl)-2-propenenitrile

시약·촉매·용매 1

HCID 962Water용매

실험 절차

β-(Thien-2-yl) acrylamide (5.2 g.) was mixed with sodium metabisulphite (12.9 g.) and heated with phosphoryl chloride (2.4 ml.) on a steam bath. After 1 hr., more phosphoryl chloride (10 ml.) was added and the mixture heated for a further 3.5 hrs. The mixture was cooled in an ice-bath and iced water cautiously added. The mixture was extracted into chloroform and the chloroform layer was washed with saturated sodium hydrogen carbonate solution, dried over sodium sulphate, and evaporated in vacuo to a brown oil. Distillation gave β-(thien-2 -yl) acrylonitrile, 1.50 g. (33%), b.p. 82- 86° /0.5 mm., λmax. (EtOH) 306 nm, (ε 18600).

후처리

  1. temperaturethe mixture heated for a further 3.5 hrs
  2. temperatureThe mixture was cooled in an ice-bath
  3. extractionThe mixture was extracted into chloroform
  4. washthe chloroform layer was washed with saturated sodium hydrogen carbonate solution
  5. dry with materialdried over sodium sulphate
  6. customevaporated in vacuo to a brown oil
  7. distillationDistillation

출처 및 근거

ORD 기록
ord-279fc58f864a40f0ace06c9667e3d612
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04012377

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