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Acetone → 3-(3-Amino-4-nitrophenyl)-1-propanol

HRID 252816
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인쇄 미리보기

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HRID 252816 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH2:11][CH2:12][CH:13]=[O:14])[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9].[BH4-].[Na+].CC(C)=O>O1CCCC1.CC(O)C.C(OCC)(=O)C>[NH2:1][C:2]1[CH:3]=[C:4]([CH2:11][CH2:12][CH2:13][OH:14])[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 180AcetoneHCID 4311764Sodium borohydrideHCID 597368753-(3-Amino-4-nitro-phenyl)-propionaldehyde

생성물 1

HCID 597367873-(3-Amino-4-nitrophenyl)-1-propanol

시약·촉매·용매 3

HCID 3776Isopropanol용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
-5 °C

실험 절차

A solution of aldehyde 80 (253 mg, 1.3 mmol) in tetrahydrofurane (1 mL) and propan-2-ol (2 mL) was treated with solid sodium borohydride (175 mg, 4.6 mmol) and stirred at −5° C. for 15 min. Acetone (5 mL) was added, stirred at the same temperature for 10 min and then diluted with ethyl acetate (100 mL), washed with 5% KHSO4 in water, then saturated NaHCO3 and finally with water, dried (MgSO4), and used for the next step without further purification.

후처리

  1. stirringstirred at the same temperature for 10 min
  2. washwashed with 5% KHSO4 in water
  3. dry with materialsaturated NaHCO3 and finally with water, dried (MgSO4)
  4. customused for the next step without further purification

출처 및 근거

ORD 기록
ord-17f881df57cc4512903ea2049bcbe2ff
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07868205B2

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
HCID 8857
Ethyl Acetate
용매