Diethyl Ether → 2-[1,3-Dithian-2-yl]-5-nitrobenzaldehyde

HRID 280710노트

반응식

HRID 280710 반응식
[S:1]1[CH2:6][CH2:5][CH2:4][S:3][CH:2]1[C:7]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][C:8]=1[CH2:9][OH:10].[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1.C(OCC)C>C(Cl)Cl>[S:1]1[CH2:6][CH2:5][CH2:4][S:3][CH:2]1[C:7]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][C:8]=1[CH:9]=[O:10]

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 135302832-[1,3-Dithian-2-yl]-5-nitrobenzyl alcoholHCID 178418287HCID 178418287, 화합물2회

생성물 1

HCID 135302842-[1,3-Dithian-2-yl]-5-nitrobenzaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 3.47 g (12.8 mmol) of the Compound 3c in methylene chloride (100 mL) was added pyridinium chlorochromate (4.15 g, 19.2 mmol). The mixture was stirred for one hour, an additional pyridinium chlorochromate (2.0 g) was added, and the mixture was stirred 15 hours. Diethyl ether (200 mL) was added to the reaction mixture, and the solvent was decanted and evaporated. The residue was purified by chromatography (silica gel, chloroform) to afford the Compound 3d as light yellow crystals; m.p. 99°-101° C.; IR 1730 cm-1 (C=O); 1H NMR δ1.7-2.3 (m,2H, --CH2CH2CH2 --), 2.8-3.3 (m, 4H,--CH2CH2CH2 --), 6.13(s, 1H, --SCHS--), 7.8-8.7 (m,--3H, ArH), 10.45 (s, 1H,CHO).

후처리

  1. stirringthe mixture was stirred 15 hours
  2. customthe solvent was decanted
  3. customevaporated
  4. customThe residue was purified by chromatography (silica gel, chloroform)

출처 및 근거

ORD 기록
ord-99d47585a5764194bb543df3f1243001
출처 데이터셋
uspto-grants-1986_05
특허 번호
US04590276

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