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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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(Dimethyl sulfide)trihydroboron → 2-(3-(Bromomethyl)-5-fluorophenyl)ethanol

HRID 446360
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HRID 446360 반응식
CSC.B.[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][C:15](O)=[O:16])[CH:10]=[C:11]([F:13])[CH:12]=1>C1COCC1>[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][CH2:15][OH:16])[CH:10]=[C:11]([F:13])[CH:12]=1
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참가 물질

4

반응물 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 579890372-(3-(Bromomethyl)-5-fluorophenyl)acetic acid

생성물 1

HCID 579893452-(3-(Bromomethyl)-5-fluorophenyl)ethanol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

Borane dimethyl sulfide complex (2M in THF, 26.3 mL) was added dropwise over 10 minutes to a solution of 2-(3-(bromomethyl)-5-fluorophenyl)acetic acid [Aromatic Intermediate 4, step a] (6.5 g) in THF (120 mL) at 0° C. The mixture was stirred at 0° C. for 10 minutes and then at 20° C. for 1 hour. The reaction mixture was quenched by dropwise addition of methanol and the solvents were removed under reduced pressure. The crude product was purified by flash silica chromatography using 30% ethyl acetate in isohexane. Fractions containing the product were concentrated to dryness to afford the titled compound. Yield 4.70 g.

후처리

  1. waitat 20° C. for 1 hour
  2. customThe reaction mixture was quenched by dropwise addition of methanol
  3. customthe solvents were removed under reduced pressure
  4. customThe crude product was purified by flash silica chromatography
  5. additionFractions containing the product
  6. concentrationwere concentrated to dryness

출처 및 근거

ORD 기록
ord-fcabc19157d144a8a8f0082cab8725a8
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08476265B2

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