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Sodium Hydroxide → HCID 54540778, 화합물

HRID 1763788
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HRID 1763788 반응식
Br[CH2:2][CH2:3][CH:4]1[O:8][C:7]([CH3:10])([CH3:9])[C:6]([CH3:12])([CH3:11])[O:5]1.[CH2:13]([NH2:19])[CH2:14][CH2:15][CH:16]=[CH:17][CH3:18].[OH-].[Na+]>O>[CH2:13]([NH:19][CH2:2][CH2:3][CH:4]1[O:8][C:7]([CH3:10])([CH3:9])[C:6]([CH3:12])([CH3:11])[O:5]1)[CH2:14][CH2:15][CH:16]=[CH:17][CH3:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 533884Hex-4-enylamineHCID 20307405HCID 20307405, 화합물

생성물 1

HCID 54540778HCID 54540778, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
100 °C

실험 절차

2-Bromoethyl-4,4,5,5-tetramethyl-1,3-dioxolane (20 grams) and 4-hexenylamine (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at a temperature of about 100° C. for a period of about 3 hours. After this time sodium hydroxide (10 grams) dissolved in water (100 ml) is added and the resulting mixture is stirred for a period of about 30 minutes. The reaction mixture is then extracted with ether. The ether extract is dried over anhydrous magnesium sulfate, filtered and stripped of solvent to yield the desired product N-hex-4-enyl-N-(4,4,5,5-tetramethyl-1,3-dioxolan-2-ylethyl)amine.

후처리

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and reflux condenser
  3. additionis added
  4. extractionThe reaction mixture is then extracted with ether
  5. extractionThe ether extract
  6. dry with materialis dried over anhydrous magnesium sulfate
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-9df2afa720794690b358f035de5e992e
출처 데이터셋
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04113464

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