Sodium Bicarbonate → HCID 58851200, 화합물

HRID 1893132노트

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HRID 1893132 반응식
[I-].[CH3:2][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[C:28]([S:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=1[CH:39]=O)([CH3:31])([CH3:30])[CH3:29].C(=O)(O)[O-].[Na+]>CCOCC>[C:28]([S:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][C:34]=1[CH:39]=[CH2:2])([CH3:31])([CH3:30])[CH3:29]

참가 물질

6

실험 절차

Methyl triphenylphosphonium iodide (1.57 g, 3.88 mmol) was dissolved in 25 ml ether in a 50 mL round-bottomed flask under dry nitrogen. To the mixture was added in one portion at 0° C. potassium tert-butoxide (0.47 g, 4.19 mmol) and it was stirred for 10 min at room temperature. 2-(tert-butylsulfanyl)benzenecarbaldehyde (2.77 mmol) was added in one portion at 0° C. and the reaction mixture was stirred until complete disappearance of the reactants (24 hr) at room temperature (followed by TLC). The mixture was added to 50 mL of saturated sodium bicarbonate solution, followed by extraction with 3×50 ml portions of ether. The extracts were dried with magnesium sulfate and evaporated. The crude product was further purified by chromatography on silica gel using petroleum ether 60-80 as eluent. 0.37 g, 70%, colorless oil. 1H NMR (200 MHz, CDCl3): δ 1.26 (s, 9H), 5.28 (dd, J1=11.0, J2=1.2, 1H), 5.68 (dd, J1=17.8, J2=1.2, 1H), 7.17-7.67 (m, 5H) ppm.

후처리

  1. stirringthe reaction mixture was stirred until complete disappearance of the reactants (24 hr) at room temperature (followed by TLC)
  2. extractionfollowed by extraction with 3×50 ml portions of ether
  3. dry with materialThe extracts were dried with magnesium sulfate
  4. customevaporated
  5. customThe crude product was further purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-7ede5de45efb4a44b396d5b805ddc0a1
출처 데이터셋
uspto-grants-2013_08
특허 번호
US08513151B2

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