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Sodium Hydroxide → HCID 53951827, 화합물

HRID 1658877
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HRID 1658877 반응식
C[O:2][C:3](=[O:18])[C:4]([CH3:17])=[CH:5][CH:6]=[CH:7][CH2:8][CH:9]([CH3:16])[CH2:10][CH2:11][CH:12]=[C:13]([CH3:15])[CH3:14].[OH-].[Na+]>CO.O>[CH3:17][C:4](=[CH:5][CH:6]=[CH:7][CH2:8][CH:9]([CH3:16])[CH2:10][CH2:11][CH:12]=[C:13]([CH3:15])[CH3:14])[C:3]([OH:18])=[O:2]
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 54097352HCID 54097352, 화합물

생성물 1

HCID 53951827HCID 53951827, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

22.8 g. of 2,7,11-trimethyl-2,4,10-dodecatrienoic acid methyl ester is dissolved in 150 ml of methanol and mixed with 22.8 g. of sodium hydroxide dissolved in 35 ml of water. The mixture is boiled under reflux for 3 hours, poured on to ice-water and extracted with diethyl ether. The ether extracts are discarded and the aqueous phase acidified with dilute sulphuric acid. The acidic aqueous solution is extracted with diethyl ether and the ether extract is washed repeatedly with aqueous sodium chloride solution, dried over sodium sulphate, filtered and concentrated on a rotary evaporator. There is obtained 2,7,11-trimethyl-2,4,10-dodecatrienoic acid.

후처리

  1. additionmixed with 22.8 g
  2. temperatureunder reflux for 3 hours
  3. extractionextracted with diethyl ether
  4. extractionThe acidic aqueous solution is extracted with diethyl ether
  5. extractionthe ether extract
  6. washis washed repeatedly with aqueous sodium chloride solution
  7. dry with materialdried over sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated on a rotary evaporator

출처 및 근거

ORD 기록
ord-2780b130f89b4a45a483a51f893ef45e
출처 데이터셋
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03966780

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