Triphenylphosphine → HCID 12988784, 화합물

HRID 353789노트

반응식

HRID 353789 반응식
N(C(OC(C)C)=O)=NC(OC(C)C)=O.[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([OH:22])=[CH:18][C:17]=1[N+:23]([O-:25])=[O:24].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O[CH2:46][CH2:47][N:48]1[CH2:53][CH2:52][O:51][CH2:50][CH2:49]1>C1COCC1>[N:48]1([CH2:47][CH2:46][O:22][C:19]2[CH:20]=[CH:21][C:16]([NH2:15])=[C:17]([N+:23]([O-:25])=[O:24])[CH:18]=2)[CH2:53][CH2:52][O:51][CH2:50][CH2:49]1

참가 물질

6

반응물 4

HCID 11776TriphenylphosphineHCID 611632-MorpholinoethanolHCID 75555Diisopropyl diazene-1,2-dicarboxylateHCID 37588824-Amino-3-Nitrophenol

생성물 1

HCID 12988784HCID 12988784, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Diisopropyl azodicarboxylate (1.1 eq) was added dropwise to a stirred solution of 4-amino-3-nitrophenol (1.0 eq), triphenylphosphine (1.1 eq), and N-(2-hydroxyethyl)morpholine (1.0 eq), in THF at 0° C. The mixture was allowed to warm to room temperature and left to stir for 18 hours. The solvent was evaporated and the product was purified by silica gel chromatography (98:2 CH2Cl2:MeOH) to yield a dark reddish-brown oil. LC/MS m/z 268.0 (MH+), Rt 1.01 minutes.

후처리

  1. waitleft
  2. customThe solvent was evaporated
  3. customthe product was purified by silica gel chromatography (98:2 CH2Cl2:MeOH)
  4. customto yield a dark reddish-brown oil

출처 및 근거

ORD 기록
ord-69260344a3c2413ba3d8ea2a6b3ec90a
출처 데이터셋
uspto-grants-2004_06
특허 번호
US06756383B2

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