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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → 3,3-Difluoro-4-methylpentane-1,4-diol

HRID 745636
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HRID 745636 반응식
[CH3:1][Li].[F:3][C:4]([F:13])([CH2:10][CH2:11][OH:12])C(OCC)=O.CC[O:16][CH2:17][CH3:18]>>[CH3:1][C:17]([OH:16])([CH3:18])[C:4]([F:13])([F:3])[CH2:10][CH2:11][OH:12]
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참가 물질

4

반응물 3

HCID 3283Diethyl EtherHCID 13189245Ethyl 2,2-difluoro-4-hydroxybutanoateHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 131892463,3-Difluoro-4-methylpentane-1,4-diol

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온도
25 °C

실험 절차

To a solution of 311 mL of 1.6M ethereal methyllithium (0.498 mol) of 0° was added dropwise 11.16 g (0.066 mol) of ethyl 2,2-difluoro-4-hydroxybutanoate in 150 mL of ether. The mixture was stirred at 0° C. for 1 hr and at 25° C. for 17 hr. The mixture was quenched by adding 14 mL of saturated brine at 0° C. The mixture was poured into saturated brine and the product was isolated with ether. The ether layers were dried over anhydrous magnesium sulfate, filtered, and evaporated to dryness. The residue was chromatographed on 0.06-0.20 mm of silica gel to give 4-methyl-3,3-difluoro-1,4-pentanediol.

후처리

  1. customThe mixture was quenched
  2. additionby adding 14 mL of saturated brine at 0° C
  3. additionThe mixture was poured into saturated brine
  4. customthe product was isolated with ether
  5. dry with materialThe ether layers were dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. customevaporated to dryness
  8. customThe residue was chromatographed on 0.06-0.20 mm of silica gel

출처 및 근거

ORD 기록
ord-8480cec98dc64fe2ae1e34f4a09358a3
출처 데이터셋
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04599330

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