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Sodium Azide → [4-(4-Azidobutyl)phenyl]acetic acid

HRID 25115
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인쇄 미리보기

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HRID 25115 반응식
[C:1]([CH2:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][CH2:12][CH2:13][CH2:14]OS(C)(=O)=O)=[CH:7][CH:6]=1)([OH:3])=[O:2].[N-:20]=[N+:21]=[N-:22].[Na+]>CN(C=O)C>[C:1]([CH2:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][CH2:12][CH2:13][CH2:14][N:20]=[N+:21]=[N-:22])=[CH:7][CH:6]=1)([OH:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 33557Sodium AzideHCID 71405718(4-{4-[(Methanesulfonyl)oxy]butyl}phenyl)acetic acid

생성물 1

HCID 22566167[4-(4-Azidobutyl)phenyl]acetic acid수율 87.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

Compound 6 (6 g, 0.02 mol) was dissolved in 80 ml of dry DMF then sodium azide (1.8 g, 0.027 mol) was added. The suspension was stirred at 80° C. (oil bath) for 3 h. The solvent was then removed at reduced pressure and the residual oil was treated with CH2Cl2 (100 mL). The resulting solution was washed with water (2×100 mL), brine and dried over magnesium sulfate. The solvent was removed under reduced pressure then the residue was redissolved in a 1:1 mixture of ethyl acetate/hexanes (200 mL) and passed through a pad of silica gel. The solvent was removed under reduced pressure to give 4.1 g (85%) of 7 as clear oil. 1H NMR (300 MHz, CDCl3) δ 1.68 (m, 4H), 2.22 (t, 2H), 3.29 (t, 3H), 3.92 (s, 3H), 7.28 (d, 2H) 7.98 (d, 2H).

후처리

  1. customThe solvent was then removed at reduced pressure
  2. additionthe residual oil was treated with CH2Cl2 (100 mL)
  3. washThe resulting solution was washed with water (2×100 mL), brine
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was removed under reduced pressure
  6. dissolutionthe residue was redissolved in a 1:1 mixture of ethyl acetate/hexanes (200 mL)
  7. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-0215e65b676e4b188998d04e38781d4c
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06858615B2

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