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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tetrahydrofuran → 22625-86-1

HRID 1153688
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HRID 1153688 반응식
O1CCC[CH2:2]1.C[Mg]Br.[C:9]([CH:12]1[CH2:17][C:16]([CH3:18])=[CH:15][CH2:14][CH2:13]1)(=[O:11])[CH3:10]>C(OCC)C>[CH3:10][C:9]([CH3:2])([CH:12]1[CH2:13][CH2:14][CH:15]=[C:16]([CH3:18])[CH2:17]1)[OH:11]
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참가 물질

5

반응물 3

HCID 8028Tetrahydrofuran2회HCID 125634641-(3-Methylcyclohex-3-en-1-yl)ethan-1-oneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 1285024522625-86-1

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
-20 °C

실험 절차

To 90 ml of dry tetrahydrofuran maintained in an inert atmosphere at -60° C. was added 45.3 ml of a 3.0M solution of methylmagnesium bromide in diethyl ether followed by dropwise addition of 15.6 g of 5-acetyl-1-methylcyclohexene in a solution of 50 ml dry tetrahydrofuran. The reaction mixture was warmed to -20° C. and stirred for two hours. The resulting reaction mixture was poured into 150 ml of chilled, saturated ammonium chloride solution and extracted three times with 300 ml portions of diethyl ether. The combined extracts were washed successively with 300 ml of water and 300 ml of saturated sodium chloride, dried (MgSO4) and concentrated in vacuo to leave 17.1 g of a pale yellow oil. Distillation of the oil gave 10.7 g of the desired product as a colorless oil, b.p. 63°-65° C. (0.65 mm).

후처리

  1. customThe resulting reaction mixture
  2. additionwas poured into 150 ml
  3. temperatureof chilled
  4. extractionsaturated ammonium chloride solution and extracted three times with 300 ml portions of diethyl ether
  5. washThe combined extracts were washed successively with 300 ml of water and 300 ml of saturated sodium chloride
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-d6b1ee314ee64a5c9efcb4c03337bda5
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04486219

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