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Diethyl Ether → 2-Ethoxy-6-pentadecyl benzaldehyde

HRID 23777
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HRID 23777 반응식
[Cr]([O-])(OCl)(=O)=O.[NH+]1C=CC=CC=1.[CH2:13]([O:15][C:16]1[CH:23]=[CH:22][CH:21]=[C:20]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38])[C:17]=1[CH2:18][OH:19])[CH3:14].CCOCC>ClCCl>[CH2:13]([O:15][C:16]1[CH:23]=[CH:22][CH:21]=[C:20]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38])[C:17]=1[CH:18]=[O:19])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 667019242-Ethoxy-6-pentadecyl-benzyl alcoholHCID 178526120HCID 178526120, 화합물

생성물 1

HCID 225745702-Ethoxy-6-pentadecyl benzaldehyde수율 83.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a 250 mL round bottom flask fitted with a reflux condenser, was added pyridinium chloro chromate (PCC) (16.1 g, 75 mmol) in anhydrous dichloromethane (100 mL). 2-Ethoxy-6-pentadecyl-benzyl alcohol (18.1 g, 50 mmol) in dichloromethane (10 mL) was added in one portion to the magnetically stirred solution. After 1.5 hr dry ether (100 mL) was added and the supernatant decanted from the black gum. The insoluble residue was washed thoroughly with diethyl ether (3×25 mL), where upon it became black granular solid. The organic solution was passed through a short pad of celite, and the solvent was removed by distillation to obtain brownish low melting solid (Yield: 15 g).

후처리

  1. customTo a 250 mL round bottom flask fitted with a reflux condenser
  2. customthe supernatant decanted from the black gum
  3. washThe insoluble residue was washed thoroughly with diethyl ether (3×25 mL), where upon it
  4. customthe solvent was removed by distillation

출처 및 근거

ORD 기록
ord-70ca60ef1c224240974ba1e40c7d798f
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06852742B2

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