2-Methyl-3-butyn-2-ol → 4-(1,1-Dimethyl-2-propynyloxy)bromobenzene

HRID 892569노트

반응식

HRID 892569 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][C:9]([CH3:12])([CH3:11])[CH:8]=[C:7](C3C=CC=C[N+]=3[O-])[C:6]=2[CH:20]=1.ClC1C=CC(C2C=CC=CC=2)=CN=1.CC(O)(C#C)C.N(C(OCC)=O)=NC(OCC)=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>ClCCl>[CH3:11][C:9]([CH3:12])([O:10][C:5]1[CH:6]=[CH:20][C:2]([Br:1])=[CH:3][CH:4]=1)[C:8]#[CH:7]

참가 물질

7

실험 절차

The 6-bromo-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran used as the starting material was prepared as follows: (A) 69.2 g of p-bromophenol and 33.6 g of 2-methylbut-3-yn-2-ol were dissolved in 600 ml of dichloromethane and 75 ml of diethyl azodicarboxylate were added. 126 g of triphenylphosphine were added portionwise and the mixture was stirred overnight. The mixture was washed with dilute hydrochloric acid and 2M sodium hydroxide solution, dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/petroleum ether (1:10) for the elution. There was obtained an oil which was distilled to give 14.4 g of 4-(1,1-dimethyl-2-propynyloxy)bromobenzene of boiling point 96°-106° C./1 mmHg. (B) In an analogous manner to that described in Example 6(A), from 4-(1,1-dimethyl-2-propynyloxy)bromobenzene and 2-iodopyridine there was obtained 6-bromo-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran.

후처리

  1. customwas prepared
  2. washThe mixture was washed with dilute hydrochloric acid and 2M sodium hydroxide solution
  3. dry with materialdried over sodium sulphate
  4. customevaporated
  5. customThe residue was chromatographed on silica gel
  6. washfor the elution
  7. customThere was obtained an oil which
  8. distillationwas distilled

출처 및 근거

ORD 기록
ord-f90d11b9f12b4a738628f048bcdcb403
출처 데이터셋
uspto-grants-1992_06
특허 번호
US05118694

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