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Methyl iodide → 8-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol methyl ether

HRID 273737
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HRID 273737 반응식
[H-].[Na+].[F:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2([OH:20])[CH2:19][CH2:18][C:13]3([O:17][CH2:16][CH2:15][O:14]3)[CH2:12][CH2:11]2)=[CH:6][CH:5]=1.I[CH3:22]>C1COCC1>[CH3:22][O:20][C:10]1([C:7]2[CH:8]=[CH:9][C:4]([F:3])=[CH:5][CH:6]=2)[CH2:11][CH2:12][C:13]2([O:14][CH2:15][CH2:16][O:17]2)[CH2:18][CH2:19]1
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 152326818-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol

생성물 1

HCID 571381988-(4-Fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol methyl ether수율 98.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
25 °C

실험 절차

Sodium hydride (1.27 g, 31.7 mmole) was added to a solution of 8-(4-fluoro-phenyl)-1,4-dioxaspiro[4.5]decan-8-ol (8.0 g, 10 mmole) in THF (100 ml) and the mixture stirred for 16 hr and heated at reflux for 4 hr. The solution was cooled to 25° C. and iodomethane (6.75 g, 47.6 mmole) was added. The mixture was stirred for 112 hr and concentrated in vacuo. The residue was suspended in water and the mixture extracted with methylene chloride. The extracts were dried and concentrated in vacuo to give 8-(4-fluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol methyl ether (98.8%, mp: 52°-54° C.).

후처리

  1. temperatureheated
  2. temperatureat reflux for 4 hr
  3. stirringThe mixture was stirred for 112 hr
  4. concentrationconcentrated in vacuo
  5. extractionthe mixture extracted with methylene chloride
  6. customThe extracts were dried
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f7f1748a0d014cf582b5653dfe57861f
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05387593

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