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Hydrochloric Acid → 1-Hydroxy-1-(3,4,5-trimethoxyphenyl)-5-hexene

HRID 618085
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인쇄 미리보기

반응식

HRID 618085 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([O:13][CH3:14])[C:10]=1[O:11][CH3:12])[CH:6]=[O:7].[CH2:15]([Mg]Br)[CH2:16][CH2:17][CH:18]=[CH2:19].Cl>O1CCCC1>[OH:7][CH:6]([C:5]1[CH:8]=[C:9]([O:13][CH3:14])[C:10]([O:11][CH3:12])=[C:3]([O:2][CH3:1])[CH:4]=1)[CH2:19][CH2:18][CH2:17][CH:16]=[CH2:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 68583,4,5-TrimethoxybenzaldehydeHCID 178445862HCID 178445862, 화합물

생성물 1

HCID 218502201-Hydroxy-1-(3,4,5-trimethoxyphenyl)-5-hexene

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

3,4,5-Trimethoxybenzaldehyde (25.48 g) was dissolved in tetrahydrofuran (50 ml), and 4-pentenylmagnesium bromide (a 1M solution in tetrahydrofuran, 200 ml) was added thereto, followed by stirring at room temperature for 30 minutes. 1N Hydrochloric acid was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give 1-hydroxy-1-(3,4,5-trimethoxyphenyl)-5-hexene (Compound VIII-1, 34.58 g)

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with a saturated saline
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3692c908b3424657a1569b2d869bb0ce
출처 데이터셋
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05952355

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