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Acetic Anhydride → (E, E)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrienyl acetate

HRID 1979545
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HRID 1979545 반응식
[CH3:1][CH:2]([CH2:6][CH2:7]/[CH:8]=[C:9](\[CH3:21])/[CH2:10][CH2:11]/[CH:12]=[C:13](\[CH3:20])/[CH2:14][CH2:15][CH:16]=[C:17]([CH3:19])[CH3:18])[CH2:3][CH2:4][OH:5].[C:22](OC(=O)C)(=[O:24])[CH3:23]>N1C=CC=CC=1>[C:22]([O:5][CH2:4][CH2:3][CH:2]([CH3:1])[CH2:6][CH2:7]/[CH:8]=[C:9](\[CH3:21])/[CH2:10][CH2:11]/[CH:12]=[C:13](\[CH3:20])/[CH2:14][CH2:15][CH:16]=[C:17]([CH3:19])[CH3:18])(=[O:24])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 5365870Geranylcitronellol

생성물 1

HCID 20246093(E, E)-3,7,11,15-Tetramethyl-6,10,14-hexadecatrienyl acetate

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

In 10 ml. of pyridine was dissolved 2.9 g. of the product obtained in Example 17, and to the solution was added 1.1 g. of acetic anhydride under stirring. The resulting mixture was then refluxed for 1 hour. The reaction mixture was then poured into 50 ml. of water, and was then extracted with n-hexane. The extract was washed with water and dried. The solvent was removed by evaporation. The residual oily product was purified by silica gel column chromatography to obtain 3.1 g. of the desired oily product.

후처리

  1. temperatureThe resulting mixture was then refluxed for 1 hour
  2. additionThe reaction mixture was then poured into 50 ml
  3. extractionof water, and was then extracted with n-hexane
  4. washThe extract was washed with water
  5. customdried
  6. customThe solvent was removed by evaporation
  7. customThe residual oily product was purified by silica gel column chromatography
  8. customto obtain 3.1 g

출처 및 근거

ORD 기록
ord-8aaceed4aa1c49d2aafde9e953103cb2
출처 데이터셋
uspto-grants-1984_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04481217

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