Sodium hydride → HCID 20287596, 화합물

HRID 127089

반응식

HRID 127089 반응식
[H-].[Na+].[C:3]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:13](=[O:17])[CH2:14][CH2:15][CH:16]=1)(O)=[O:4].C(Cl)(=O)C([Cl:21])=O>O1CCCC1.CCOCC>[Cl:21][C:3]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][C:12]1[C:13](=[O:17])[CH2:14][CH2:15][CH:16]=1)=[O:4]

참가 물질

6

반응물 3

HCID 24758Sodium hydrideHCID 65578Oxalyl chlorideHCID 789025-Oxo-1-cyclopentene-1-heptanoic acid

생성물 1

HCID 20287596HCID 20287596, 화합물

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
0 °C

실험 절차

To a suspension of 1.94 g (0.08 mol) of sodium hydride in 100 ml of tetrahydrofuran is added with stirring under argon dropwise a solution of 17 g (0.08 mol) of 2-(6-carboxyhexyl)cyclopent-2-en-1-one in 160 ml of tetrahydrofuran. After the addition is complete, the mixture is stirred for 1 hour 15 minutes. The mixture is cooled to 0° C. and 13 ml of oxalyl chloride is added. The mixture is stirred at 0° C. for 30 minutes and at room temperature for 30 minutes. The solution is diluted with 500 ml of ether and filtered through Celite. The solvent is removed from the filtrate and the residue is extracted with hot hexane twice. The hexane is removed to give 16.0 g of the title compound.

후처리

  1. additionis added
  2. additionAfter the addition
  3. stirringThe mixture is stirred at 0° C. for 30 minutes and at room temperature for 30 minutes
  4. filtrationfiltered through Celite
  5. customThe solvent is removed from the filtrate
  6. extractionthe residue is extracted with hot hexane twice
  7. customThe hexane is removed

출처 및 근거

ORD 기록
ord-1ae4d7594c9d4be0af8f2fd7dc9e0ea2
출처 데이터셋
uspto-grants-1981_03
특허 번호
US04254285

연결된 노트

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