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Sodium borohydride → HCID 58565346, 화합물

HRID 2175327
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HRID 2175327 반응식
[F:1][C:2]1[CH:3]=[C:4]([N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH:10]=[C:9]2[C:17](=[O:19])[CH3:18])[CH:5]=[CH:6][CH:7]=1.[BH4-].[Na+]>CO>[F:1][C:2]1[CH:3]=[C:4]([N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH:10]=[C:9]2[CH:17]([OH:19])[CH3:18])[CH:5]=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 58565344HCID 58565344, 화합물

생성물 1

HCID 58565346HCID 58565346, 화합물수율 92.6%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a mixture of 1-[1-(3-fluorophenyl)-1H-indol-2-yl]ethanone (0.27 g, 1.1 mmol) in methanol (6 mL) was added sodium tetrahydroborate (41 mg, 1.1 mmol). The reaction was stirred at room temperature for 1 hour, quenched with water, and extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4 and concentrated to give title compound (0.26 g). The crude product was used directly in the next step. LCMS calculated for C16H13FN(M-OH)+: m/z=238.1. Found: 238.1.

후처리

  1. customquenched with water
  2. extractionextracted with EtOAc
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-60821f8ad1fa49eeaea5332fca0ac192
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09062055B2

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