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Sodium cyanoborohydride → HCID 66632922, 화합물

HRID 915675
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HRID 915675 반응식
[C:1]1([C:7]2[CH:8]=[C:9]([CH:12]=O)[O:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BH3-]C#[N:16].[Na+]>CO>[C:1]1([C:7]2[CH:8]=[C:9]([CH2:12][NH2:16])[O:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5003444Sodium cyanoborohydrideHCID 1354168999113-85-6

생성물 1

HCID 66632922HCID 66632922, 화합물수율 21.8%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Prepare a solution of 4-phenyl-2-formylfuran (1.5 g, 8.7 mmol) and MeOH (35 mL). Add NH4OAc (6.7 g, 87.1 mmol) and NaCNBH3 (380 mg, 6.1 mmol). Stir the reaction mixture under nitrogen for 12 hours. Upon completion of the reaction, concentrate the resulting mixture, dilute with water (10 mL), basify with 1 N sodium hydroxide, and extract with diethyl ether (2×10 mL). Dry the organic phase (Na2SO4), filter, and concentrate. Perform flash chromatography on silica gel eluting with 9:1 ethyl acetate/MeOH to afford the title compound (230 mg) as a white solid. 1H NMR (CDCl3) δ 7.65 (s, 1H), 7.46 (d, J=7 Hz, 1H), 7.36 (t, J=7 Hz, 1H), 7.26 (m, 1H), 6.49 (s, 1H), 3.89 (s, 2H), 2.10 (s, 2H).

후처리

  1. customUpon completion of the reaction
  2. concentrationconcentrate the resulting mixture
  3. additiondilute with water (10 mL), basify with 1 N sodium hydroxide
  4. extractionextract with diethyl ether (2×10 mL)
  5. dry with materialDry the organic phase (Na2SO4)
  6. filtrationfilter
  7. concentrationconcentrate

출처 및 근거

ORD 기록
ord-b06ea2a4ed944febabde7472e84a33b9
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07265246B2

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