Triphenylphosphine → 5-Ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furan

HRID 865696

반응식

HRID 865696 반응식
N(C(OCC)=O)=NC(OCC)=O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:32]([C:34]1[O:38][C:37]([CH2:39][CH2:40][CH2:41][OH:42])=[CH:36][CH:35]=1)[CH3:33].[CH3:43][N:44]1[N:48]=[N:47][C:46]([C:49]2[CH:54]=[C:53]([CH3:55])[C:52](O)=[C:51]([CH3:57])[CH:50]=2)=[N:45]1>O>[CH2:32]([C:34]1[O:38][C:37]([CH2:39][CH2:40][CH2:41][O:42][C:52]2[C:51]([CH3:57])=[CH:50][C:49]([C:46]3[N:47]=[N:48][N:44]([CH3:43])[N:45]=3)=[CH:54][C:53]=2[CH3:55])=[CH:36][CH:35]=1)[CH3:33]

참가 물질

6

반응물 4

HCID 11776TriphenylphosphineHCID 148372Win 58768HCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 229154015-Ethyl-2-(3-hydroxypropyl)furan2회

생성물 1

HCID 159546435-Ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furan수율 65.4%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Diethyl azodicarboxylate (DEAD, 4.84 g; 27.8 mmol) was added under nitrogen to a stirred and cooled (-20° C.) solution of triphenylphosphine (7.37 g; 27.8 mmol), 5-ethyl-2-(3-hydroxypropyl)furan (Intermediate 1c) (3.9 g; 25.3 mmol), and 4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenol (5.69 g; 27.8 mmol). The mixture was stirred at -20° C. for 1/2 h, and then was allowed to warm to room temperature overnight. Water (50 mL) was added to the mixture and the layers were separated. The aqueous layer was extracted with ether (3×50 mL), the organic layer was washed with 10% NaOH solution (3×50 mL), water, and dried over magnesium sulfate. The solvent was concentrated in vacuo to yield a residue and purified by MPLC column chromatography (ethyl acetate/hexane, 3:7) to afford 5.63 g (65%) of 5-ethyl-2-[3-[2,6-dimethyl-4-(2-methyl-tetrazol-5-yl)-phenoxy]-propyl]furan (Formula II; R3 =5-ethyl, R4 =hydrogen, R1, R2 =3,5-dimethyl, R5 =2-methyltetrazol-5-yl, Y=1,3-propylene).

후처리

  1. stirringThe mixture was stirred at -20° C. for 1/2 h
  2. customthe layers were separated
  3. extractionThe aqueous layer was extracted with ether (3×50 mL)
  4. washthe organic layer was washed with 10% NaOH solution (3×50 mL), water
  5. dry with materialdried over magnesium sulfate
  6. concentrationThe solvent was concentrated in vacuo
  7. customto yield a residue
  8. custompurified by MPLC column chromatography (ethyl acetate/hexane, 3:7)

출처 및 근거

ORD 기록
ord-5d747741ff1f4beda690ecf2fbb749f3
출처 데이터셋
uspto-grants-1996_10
특허 번호
US05567717

연결된 노트

불러오는 중…