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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 1-Methoxy-4-(1-methylethenyl)benzene

HRID 392550
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HRID 392550 반응식
C[Mg]Br.[CH2:4](OCC)C.[CH3:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([C:17](=O)[CH3:18])=[CH:13][CH:12]=1.Cl>C(OCC)C>[CH3:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]([CH3:18])=[CH2:4])=[CH:13][CH:12]=1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 74764'-MethoxyacetophenoneHCID 178467822HCID 178467822, 화합물

생성물 1

HCID 2594141-Methoxy-4-(1-methylethenyl)benzene

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

To a 1000 mL three-necked flask equipped with a mechanical stirrer, methyl magnesium bromide/diethyl ether solution (200 mL, 3.0 mol) is added. A solution of 85.3 g of 4′-methoxy-acetophenone dissolved in 80 mL of anhydrous diethyl ether is charged to the Grignard reagent over 90 minutes at ambient temperature. Diethyl ether (200 mL) and 250 mL of 3N hydrochloric acid are added slowly to the reaction mixture. The solution is stirred for another 30 minutes. The aqueous layer is separated and washed twice with 100 mL of diethyl ether. The ethereal layers are combined and vacuum distilled. The desired product is obtained in a yield of 91.7 g as a yellow oil whose structure is verified by 1Hnmr and mass spectroscopy.

후처리

  1. customTo a 1000 mL three-necked flask equipped with a mechanical stirrer
  2. customThe aqueous layer is separated
  3. washwashed twice with 100 mL of diethyl ether
  4. distillationvacuum distilled

출처 및 근거

ORD 기록
ord-c3c4cde8356b49bb88c14ecf0ba94844
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06800676B2

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