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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl Bromide → 65755-78-4

HRID 1413085
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HRID 1413085 반응식
[Na].[CH2:2](Br)[CH3:3].[CH:5]1([C:13]#[N:14])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1>N>[CH2:2]([C:5]1([C:13]#[N:14])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1)[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6332Ethyl BromideHCID 5360545SodiumHCID 13075060cyclooctanecarbonitrile

생성물 1

HCID 2054921165755-78-4

시약·촉매·용매 1

HCID 222Ammonia용매2회

실험 절차

Sodium (3.7 g, 0.16 mole) was added to liquid ammonia (300 ml.) at 35° C. A catalytic amount of ferric nitrate was then added. After the solution had become grey in colour, ethyl bromide (17.4 g, 0.16 mole) and cyclooctyl cyanide (20.0 g, 0.14 mole) were added very slowly. The liquid ammonia was then allowed to evaporate over a period of 20 hours. Benzene and then water were added to the residue. The benzene layer was dried (MgSO4) and distilled to give 1-ethylcyclooctyl cyanide, bp. 130°-132°/17 mm.

후처리

  1. additionwere added very slowly
  2. customto evaporate over a period of 20 hours
  3. additionBenzene and then water were added to the residue
  4. dry with materialThe benzene layer was dried (MgSO4)
  5. distillationdistilled

출처 및 근거

ORD 기록
ord-0d7e82cf26d74d228bd0b1c035498721
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04248859

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