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Sodium borohydride → Ethyl 3-(hydroxy(phenyl)methyl)benzoate

HRID 1254242
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HRID 1254242 반응식
[C:1]([C:9]1[CH:10]=[C:11]([CH:17]=[CH:18][CH:19]=1)[C:12]([O:14][CH2:15][CH3:16])=[O:13])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>C(O)C>[OH:8][CH:1]([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:9]1[CH:10]=[C:11]([CH:17]=[CH:18][CH:19]=1)[C:12]([O:14][CH2:15][CH3:16])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 14789261Ethyl 3-benzoylbenzoate

생성물 1

HCID 57544858Ethyl 3-(hydroxy(phenyl)methyl)benzoate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of ethyl 3-benzoylbenzoate (1.0197 g, 4.0 mmol, 1.0 equiv) in ethanol (10 mL) was added of NaBH4 (0.32 g, 2.1 equiv). The reaction mixture was stirred at rt for 1.5 h, quenched with 10% aq Na2CO3, extracted three times with CH2Cl2, and dried over Na2SO4. The crude product was used in the next step without further purification. LC-MS (3 min) tR=1.64 min, m/z 239 (M+-OH). 1H NMR (400 MHz, CDCl3) δ 8.09 (m, 1H), 7.93-7.96 (m, 1H), 7.56-7.59 (m, 1H), 7.26-7.43 (m, 6H), 5.89 (s, 1H), 4.36 (q, J=7.2 Hz, 2H), 2.38 (br s, 1H), 1.40 (t, J=7.2 Hz, 3H).

후처리

  1. customquenched with 10% aq Na2CO3
  2. extractionextracted three times with CH2Cl2
  3. dry with materialdried over Na2SO4
  4. customThe crude product was used in the next step without further purification
  5. customLC-MS (3 min) tR=1.64 min, m/z 239 (M+-OH)

출처 및 근거

ORD 기록
ord-4c4a669df9ce4d91baa0472c6a282894
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08455521B2

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