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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Hexanol → (R)-(+)-2,3-EPOXYPROPYL HEXYL ETHER

HRID 1886303
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HRID 1886303 반응식
[CH2:1]([OH:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[OH-].[Na+].[CH2:10]([C@@H:12]1[O:14][CH2:13]1)Cl>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.O>[CH2:1]([O:7][CH2:10][C@@H:12]1[O:14][CH2:13]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 81031-HexanolHCID 14798Sodium HydroxideHCID 2734062(-)-Epichlorohydrin

생성물 1

HCID 36691064(R)-(+)-2,3-EPOXYPROPYL HEXYL ETHER

시약·촉매·용매 2

HCID 94433Tetrabutylammonium hydrogen sulfate촉매HCID 962Water용매

실험 절차

6 ml of n-hexanol was added dropwise to a mixture of 40 g of 50% sodium hydroxide solution, 24 g of (R)-epichlorohydrine as used in the Synthetic Example 1 and 400 mg of tetrabutylammoniumhydrogen sulfate, under cooling at 20° to 25° C. The reaction solution was stirred at the same temperature for 3 hours and added with water, and then the product was extracted into ether. The extracted product was distilled under reduced pressure to obtain 3.35 g of (R)-n-hexylglycidylether.

후처리

  1. temperatureunder cooling at 20° to 25° C
  2. extractionthe product was extracted into ether
  3. distillationThe extracted product was distilled under reduced pressure

출처 및 근거

ORD 기록
ord-b780f9ff94fe42f39fca6cc855ac2e19
출처 데이터셋
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05151214

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