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1,2-Dimethoxyethane → HCID 54138531, 화합물

HRID 979981
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HRID 979981 반응식
[H-].[Na+].[N:3]1[C:16]2[NH:15][C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[S:8][C:7]=2[N:6]=[CH:5][CH:4]=1.C[C:18]#[C:19][C:20]([O-:22])=[O:21].[CH2:23](COC)OC>>[C:20]([CH:19]=[CH:18][N:15]1[C:16]2[N:3]=[CH:4][CH:5]=[N:6][C:7]=2[S:8][C:9]2[C:14]1=[CH:13][CH:12]=[CH:11][CH:10]=2)([O:22][CH3:23])=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 80711,2-DimethoxyethaneHCID 24758Sodium hydrideHCID 6994510HCID 6994510, 화합물HCID 12351784HCID 12351784, 화합물

생성물 1

HCID 54138531HCID 54138531, 화합물

실험 절차

To a suspension of sodium hydride (0.1 g, 4.2 mmoles) in dimethoxyethane (10 ml) was added 1,4-diazaphenothiazine (200 mg, 1 mmole). After stirring for 30 minutes a deep red solution of the anion was obtained and this was treated with methylpropiolate (85 μl, 1.0 mmole). Stirring was maintained for 30 minutes. The mixture was evaporated to dryness and the residue was purified by chromatography. Elution with 40% EtOAc/hexane gave the desired product as on orange solid, m.p. 165°-169°. NMR analysis showed the product to be a mixture of trans and cis isomers in a ratio of 4 to 1.

후처리

  1. customwas obtained
  2. stirringStirring
  3. temperaturewas maintained for 30 minutes
  4. customThe mixture was evaporated to dryness
  5. customthe residue was purified by chromatography
  6. washElution with 40% EtOAc/hexane

출처 및 근거

ORD 기록
ord-b000da798df54451ad7d1f056ecf7daf
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04634766

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