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Diethyl Ether → HCID 18182277, 화합물

HRID 1359414
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HRID 1359414 반응식
C(OCC)C.[CH2:6]([C:13]1[C:14]2[CH2:21][CH2:20][CH:19]([C:22](OCC)=[O:23])[CH2:18][C:15]=2[S:16][CH:17]=1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+]>O>[CH2:6]([C:13]1[C:14]2[CH2:21][CH2:20][CH:19]([CH2:22][OH:23])[CH2:18][C:15]=2[S:16][CH:17]=1)[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3283Diethyl Ether2회HCID 14798Sodium HydroxideHCID 18182320HCID 18182320, 화합물HCID 21226445Aluminium lithium hydride

생성물 1

HCID 18182277HCID 18182277, 화합물

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A solution of 10 ml of diethyl ether containing 2.8 g of 3-benzyl-6-ethoxycarbonyl-4,5,6,7-tetrahydrobenzo[b]thiophene was slowly added dropwise into a suspension of 100 ml of diethyl ether containing 421 mg of lithium aluminum hydride under ice-cooling. After stirring as it was for 30 minutes, 0.4 ml of water, 0.4 ml of an aqueous 1N sodium hydroxide solution and 0.4 ml of water were successively added to the reaction solution and the mixture was dried over anhydrous magnesium sulfate. After filtering, the solvent was removed, to give 2.5 g of the target compound.

후처리

  1. temperaturecooling
  2. dry with materialthe mixture was dried over anhydrous magnesium sulfate
  3. filtrationAfter filtering
  4. customthe solvent was removed

출처 및 근거

ORD 기록
ord-a1a82b284aee4522bc59eeb794be5fc2
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06599917B1

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