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Hydrochloric Acid → 2,5,9,12-Tetraoxatridecan-7-ol

HRID 567644
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HRID 567644 반응식
[CH3:1][O:2][CH2:3][CH2:4][OH:5].[OH-].[Na+].[CH3:8][O:9][CH2:10][CH2:11][O:12][CH2:13][CH:14]1[O:16][CH2:15]1.Cl>CC(C)=O>[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:15][CH:14]([OH:16])[CH2:13][O:12][CH2:11][CH2:10][O:9][CH3:8]
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 80192-MethoxyethanolHCID 14798Sodium Hydroxide2회HCID 2347342-((2-Methoxyethoxy)methyl)oxirane

생성물 1

HCID 148932732,5,9,12-Tetraoxatridecan-7-ol수율 85%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
80 °C

실험 절차

To ethylene glycol monomethyl ether (86.4 g, 2.27 moles), ground caustic soda (16.7 g, 0.83 moles) was added by several portions and caustic soda was dissolved by heating to 80° C. Ethylene glycol glycidyl methyl ether (50 g, 0.76 moles) was then added dropwise. After the completion of the dropwise addition, the solution was stirred for 2 hours and then air-cooled at room temperature. The solution was neutralized with hydrochloric acid and a salt was deposited by adding acetone, followed by filtration. Low-boiling materials were removed under reduced pressure to obtain 67 g (yield 85%) of 1,3-bis(2-methoxyethoxy)-2-propanol.

후처리

  1. dissolutionwas dissolved
  2. additionAfter the completion of the dropwise addition
  3. temperatureair-cooled at room temperature
  4. filtrationfollowed by filtration
  5. customwere removed under reduced pressure

출처 및 근거

ORD 기록
ord-b57ab0857f8a43b79376294d8d1e38af
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06180287B2

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