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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 10877568, 화합물

HRID 2352501
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HRID 2352501 반응식
[CH3:1][Si:2]([CH3:17])([CH3:16])[C:3]#[C:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9]C1CCCCO1.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>CO>[CH3:17][Si:2]([CH3:1])([CH3:16])[C:3]#[C:4][CH2:5][CH2:6][CH2:7][CH2:8][OH:9]
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참가 물질

4

반응물 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 14652360HCID 14652360, 화합물

생성물 1

HCID 10877568HCID 10877568, 화합물수율 73.6%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1-Trimethylsilyl[6-(oxacyclohex-2-yloxy)]hex-1-yne (76 g, 300 mmol) and pyridinium p-toluenesulfonate (0.05 g) were heated at reflux in methanol (200 mL). After cooling the solvent was removed under reduced pressure, the residue was dissolved in methylene chloride and washed with water, brine and dried (MgSO4). Evaporation of the solvent under reduced pressure afforded a residue which was distilled (b.p. 96° C., 3 mm Hg) to give 37.6 g (64%) of the product.

후처리

  1. temperatureAfter cooling the solvent
  2. customwas removed under reduced pressure
  3. dissolutionthe residue was dissolved in methylene chloride
  4. washwashed with water, brine
  5. dry with materialdried (MgSO4)
  6. customEvaporation of the solvent under reduced pressure
  7. customafforded a residue which
  8. distillationwas distilled (b.p. 96° C., 3 mm Hg)

출처 및 근거

ORD 기록
ord-bd69a0667ac1498f804d7bed6fd4d07d
출처 데이터셋
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04877779

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