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Triethylamine → 3-Nitrooxy-propyl 5-nitrooxy-hexanoate

HRID 1776951
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인쇄 미리보기

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HRID 1776951 반응식
[N+:1]([O:4][CH2:5][CH2:6][CH2:7][OH:8])([O-:3])=[O:2].[CH2:9](N(CC)CC)C.[N+:16]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][C:24](Cl)=[O:25])([O-:18])=[O:17]>C(OCC)C>[N+:16]([O:19][CH:20]([CH3:9])[CH2:21][CH2:22][CH2:23][C:24]([O:8][CH2:7][CH2:6][CH2:5][O:4][N+:1]([O-:3])=[O:2])=[O:25])([O-:18])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 100118933-NitrooxypropanolHCID 212769385-Chloro-5-oxopentyl nitrate

생성물 1

HCID 885402503-Nitrooxy-propyl 5-nitrooxy-hexanoate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

20 mmol 3-Nitrooxypropanol dissolved in 10 ml Diethylether and 20 mmol Triethylamine were cooled to 0° C. 18.2 mmol 5-nitrooxypentoylchlorid were dropped over a period of 5 min at 0 to 5° C. After stirring over night without cooling, the reaction mixture was extracted with 1N HCl, twice with water, washed with brine, dried over Na2SO4 and the solvent was removed in vacuo.

후처리

  1. temperaturewithout cooling
  2. extractionthe reaction mixture was extracted with 1N HCl, twice with water
  3. washwashed with brine
  4. dry with materialdried over Na2SO4
  5. customthe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-e5e42d10eb7045f9a12bc42b292b08fb
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09266814B2

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