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Nitric Acid → 5-(Benzyloxy)-4-methoxy-2-nitrobenzonitrile

HRID 1003998
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HRID 1003998 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][C:16]=1[O:17][CH3:18])[C:12]#[N:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N+:19]([O-])([OH:21])=[O:20].O>C(O)(=O)C>[CH2:1]([O:8][C:9]1[C:16]([O:17][CH3:18])=[CH:15][C:14]([N+:19]([O-:21])=[O:20])=[C:11]([CH:10]=1)[C:12]#[N:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 962WaterHCID 27522763-(Benzyloxy)-4-methoxybenzonitrile

생성물 1

HCID 110333845-(Benzyloxy)-4-methoxy-2-nitrobenzonitrile수율 68%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A solution of 3-benzyloxy-4-methoxybenzonitrile (43.8 g, 0.18 mol) in glacial acetic acid (87 ml) was added dropwise to concentrated nitric acid (70% w/w, 244 ml) with periodic cooling to maintain the reaction temperature below 30° C. Once the addition was complete, the reaction was stirred for a further 30 minutes, after which time the mixture was poured into water (11) and stirred for 30 minutes. The resulting precipitate was isolated by filtration, washed with water and dried under reduced pressure at 50° C. to afford the subtitle compound as a white solid (35.1 g, 68%). Rf 0.70 (EtOAc:hexane 1:1, v/v).

후처리

  1. temperaturewith periodic cooling
  2. temperatureto maintain the reaction temperature below 30° C
  3. additionOnce the addition
  4. stirringstirred for 30 minutes
  5. customThe resulting precipitate was isolated by filtration
  6. washwashed with water
  7. customdried under reduced pressure at 50° C.

출처 및 근거

ORD 기록
ord-135a3717637a440193c0b4d4ffff8d6a
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06048864

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