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Ethyl chloroacetate → 2,6,10-Trimethylundeca-5,9-dienal

HRID 1578809
노트
인쇄 미리보기

반응식

HRID 1578809 반응식
[CH2:1]([CH2:11]C(=O)C)/[CH:2]=[C:3](/[CH2:5][CH2:6][CH:7]=[C:8]([CH3:10])[CH3:9])\[CH3:4].ClCC([O:19][CH2:20][CH3:21])=O.[O-][CH2:23]C.[Na+].[OH-].[K+]>CO.C(O)(=O)C.O>[CH3:23][CH:21]([CH2:11][CH2:1][CH:2]=[C:3]([CH3:4])[CH2:5][CH2:6][CH:7]=[C:8]([CH3:9])[CH3:10])[CH:20]=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 7751Ethyl chloroacetateHCID 14797Potassium HydroxideHCID 1549778GeranylacetoneHCID 2723922Sodium ethoxide

생성물 1

HCID 911152,6,10-Trimethylundeca-5,9-dienal수율 73.6%

시약·촉매·용매 3

HCID 176Acetic Acid용매
HCID 887
Methanol
용매
HCID 962Water용매2회

실험 절차

To a mixture of geranylacetone (171 g) and ethyl monochloroacetate (141 g) at -10°C in the nitrogen stream, sodium ethoxide (71 g) is portionwise added, and the resultant mixture is stirred for 6 hours. A solution of potassium hydroxide (99 g) in methanol (560 ml) is added thereto, and stirring is continued for 2 hours. The reaction mixture is poured into water and skaken with petroleum ether. The water layer is neutralized with acetic acid and extracted with ether. The ether extract is washed with water and dried. After evaporation of the ether, the residual material is distilled under reduced pressure to give 2,6,10-trimethyl-5,9-undecadienal (135 g) as a pale yellow oil. B.P. 100° to 103°C/0.4 mm Hg. Yield, 73.6%. IR: 2680, 1720 cm-1 (CHO).

후처리

  1. additionis portionwise added
  2. extractionextracted with ether
  3. extractionThe ether extract
  4. washis washed with water
  5. customdried
  6. customAfter evaporation of the ether
  7. distillationthe residual material is distilled under reduced pressure

출처 및 근거

ORD 기록
ord-6345e99ee7ec4564936dd8c683feea50
출처 데이터셋
uspto-grants-1976_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03939202

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