홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Ethyl Bromide → HCID 68841469, 화합물

HRID 1948609
노트
인쇄 미리보기

반응식

HRID 1948609 반응식
[CH2:1](Br)C.BrC1C=NC=CC=1.[Mg].[CH3:12][N:13]([CH3:26])[C:14]1([C:24]#N)[CH2:23][CH2:22][C:17]2([O:21][CH2:20][CH2:19][O:18]2)[CH2:16][CH2:15]1.[Cl-:27].[NH4+]>C(OCC)C.C1COCC1.O>[ClH:27].[CH2:24]([C:14]1([N:13]([CH3:26])[CH3:12])[CH2:23][CH2:22][C:17]2([O:21][CH2:20][CH2:19][O:18]2)[CH2:16][CH2:15]1)[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 6332Ethyl BromideHCID 122863-BromopyridineHCID 25517Ammonium ChlorideHCID 3609778-(Dimethylamino)-1,4-dioxaspiro[4.5]decane-8-carbonitrileHCID 5462224Magnesium

생성물 1

HCID 68841469HCID 68841469, 화합물

시약·촉매·용매 3

HCID 962
Water
용매
HCID 3283Diethyl Ether용매2회
HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of ethyl bromide (30.0 g, 0.3 mole) and 3-bromopyridine (16.0 g, 0.1 mole) was added dropwise to magnesium powder (10.0 g) in diethyl ether (50 ml). After the Grignard reaction had gone to completion, 8-dimethylamino-1,4-dioxa-spiro[4.5]decane-8-carbonitrile (10.5 g, 47.6 mmole) in THF (80 ml) was added within 15 minutes at 0° C. to the grey solution and the mixture was stirred overnight at RT. 20% ammonium chloride solution (50 ml) and water (50 ml) were then added to the reaction solution while cooling with ice. The reaction solution was diluted with diethyl ether (100 ml), and the organic phase was separated and the aqueous phase was extracted twice with Et2O (100 ml). The combined organic phases were washed with water (50 ml) and NaCl solution (50 ml), dried over Na2SO4, filtered and the solvent was removed in vacuo. The residue was taken up in 2-butanone (200 ml) and Me3SiCl (10 ml) was added at 0° C. The reaction solution was stirred for 5 hours under exclusion of moisture and the precipitated solid was suction filtered.

후처리

  1. customAfter the Grignard reaction
  2. additionwas added within 15 minutes at 0° C. to the grey solution
  3. temperaturewhile cooling with ice
  4. customthe organic phase was separated
  5. extractionthe aqueous phase was extracted twice with Et2O (100 ml)
  6. washThe combined organic phases were washed with water (50 ml) and NaCl solution (50 ml)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customthe solvent was removed in vacuo
  10. additionMe3SiCl (10 ml) was added at 0° C
  11. stirringThe reaction solution was stirred for 5 hours under exclusion of moisture
  12. filtrationfiltered

출처 및 근거

ORD 기록
ord-0c32783ac96b48eb8cf2d32cad505376
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399503B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트