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Phosphorus oxychloride → HCID 13013934, 화합물

HRID 444147
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HRID 444147 반응식
O=[C:2]1[C:8]2[CH:9]=[CH:10][C:11]([C:13]([O:15][CH3:16])=[O:14])=[CH:12][C:7]=2[S:6](=[O:18])(=[O:17])[C:5]2[CH:19]=[CH:20][CH:21]=[CH:22][C:4]=2[NH:3]1.P(Cl)(Cl)(Cl)(Cl)[Cl:24].P(Cl)(Cl)(Cl)=O>>[Cl:24][C:2]1[C:8]2[CH:9]=[CH:10][C:11]([C:13]([O:15][CH3:16])=[O:14])=[CH:12][C:7]=2[S:6](=[O:18])(=[O:17])[C:5]2[CH:19]=[CH:20][CH:21]=[CH:22][C:4]=2[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 13013925HCID 13013925, 화합물

생성물 1

HCID 13013934HCID 13013934, 화합물

실험 절차

Add 6.34 gm. (20 mmole) of finely powdered methyl 10,11-dihydro-11-oxodibenzo[b,f][1,4]thiazepin-3-carboxylate 5,5-dioxide to a mixture of 6.25 gm. (30 mmole) phosphorous pentachloride in 17.3 ml. of phosphoryl chloride. Stir for 18 hours at room temperature. Separate the solids by filtration, wash with ether and dry in vacuo over potassium hydroxide. Dissolve the crude product in boiling tetrahydrofuran, filter and evaporate to a small volume in a stream of nitrogen. Dilute with acetonitrile and separate the precipitate by filtration in order to obtain the title product. (m.p. 254°-256° C.).

후처리

  1. additionAdd 6.34 gm
  2. customSeparate the solids
  3. filtrationby filtration
  4. washwash with ether
  5. dry with materialdry in vacuo over potassium hydroxide
  6. dissolutionDissolve the crude product
  7. filtrationfilter
  8. customevaporate to a small volume in a stream of nitrogen
  9. additionDilute with acetonitrile
  10. customseparate the precipitate
  11. filtrationby filtration in order

출처 및 근거

ORD 기록
ord-b855f97bd9b04ae8b666ed221685351c
출처 데이터셋
uspto-grants-1981_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04263207

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