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Water → HCID 54087283, 화합물

HRID 981012
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HRID 981012 반응식
[CH:1]1([OH:14])[CH2:12][CH2:11][CH:10]=[CH:9][CH2:8][CH2:7][CH:6]=[CH:5][CH2:4][CH2:3][CH:2]1[OH:13].[CH3:15][CH2:16][CH2:17][CH2:18][CH:19]=O.C1(C)C=CC(S(O)(=O)=O)=CC=1.O>[Cl-].[Na+].O>[CH2:16]([CH:15]1[O:13][CH:2]2[CH:1]([CH2:12][CH2:11][CH:10]=[CH:9][CH2:8][CH2:7][CH:6]=[CH:5][CH2:4][CH2:3]2)[O:14]1)[CH2:17][CH2:18][CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6101p-Toluenesulfonic acidHCID 8063PentanalHCID 107382HCID 107382, 화합물

생성물 1

HCID 54087283HCID 54087283, 화합물수율 90%

시약·촉매·용매 1

HCID 57417360Sodium chloride; water용매

실험 절차

5 g of 5,9-cyclododecadien-1,2-diol, 2.4 g of valeric aldehyde, a spatula of p-toluenesulfonic acid and 200 ml of 80/100 petroleum ether were charged into a 250 ml two-neck flask equipped with a water separator and the mixture was taken to reflux for 1 h. The reaction mixture was then poured on ice, neutralized with brine, dried and concentrated. Distillation in a bulb-to-bulb apparatus produced 6.06 g of 14-butyl-13,15-dioxabicyclo[10.3.0]pentadeca-4,8-diene.

후처리

  1. temperatureto reflux for 1 h
  2. additionThe reaction mixture was then poured on ice
  3. customdried
  4. concentrationconcentrated
  5. distillationDistillation in a bulb-to-bulb apparatus

출처 및 근거

ORD 기록
ord-7ed73a277c27453eb32791a42960d9ec
출처 데이터셋
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04990495

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