Monobenzone → (S)-p-Benzyloxy-(1-methylheptyloxy)benzene

HRID 2257438

反応式

HRID 2257438 の反応式
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:35][C@@H:36](O)[CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42].N(C(OCC)=O)=NC(OCC)=O>ClCCl.O>[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([O:15][C@@H:36]([CH3:35])[CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42])=[CH:13][CH:14]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

7

反応物 4

HCID 7638MonobenzoneHCID 11776TriphenylphosphineHCID 80080(R)-2-OctanolHCID 220568ethyl N-ethoxycarbonyliminocarbamate

生成物 1

HCID 53745214(S)-p-Benzyloxy-(1-methylheptyloxy)benzene収率 71%

試薬・触媒・溶媒 2

HCID 962Water触媒HCID 6344Dichloromethane溶媒3 回

実験手順

To an argon-flushed flask containing a solution of 3.01 g (15 mmol) of p-benzyloxy-phenol and 1.25 eq of triphenylphosphine in 220 ml in dry dichloromethane, was added a solution of 4.91 g (15.14 mmol) of (R)-2-octanol in 30 ml of dry dichloromethane via syringe. Then 1.20 eq of diethyl azodicarboxylate dissolved in 60 ml of dry dichloromethane was added dropwise for 30 min. The reaction mixture was stirred at room temperature for 19 h, Then 5 drops of water were added and the mixture was stirred for 1 h. The solvent was then evaporated and the residual crude product was triturated in a mixture of hexanes/ethyl acetate [70/30] for 1 h and filtered through a short silica gel pad. The filtrate was evaporated and the product was purified by flash chromatography on silica gel using dichloromethane/hexanes [10/90] as eluent, affording 3.32 g (71%) of (S)-p-Benzyloxy-(1-methylheptyloxy)benzene (Compound 18, Scheme III, R2 =(S)-OCH(CH3)C6H13) as a colorless liquid: Rf [dichloromethane/hexanes 10/90]: 0.13; 1H NMR (300 MHz, CDCl3): δ 0.87(t, 3H, J=6.6 Hz), 1.20-1.60(m, 12H), 1.70(m, 1H), 4.21(m, 1H), 5.00(s, 2H), Distorted AA'BB' System [6.82(d, 2H) 6.88(d, 2H)], 7.30-7.46(m, 5H); 13C NMR (300 MHz, CDCl3): δ 14.02, 19.77, 22.55, 25.52, 29.26, 31.77, 36.51, 70.63, 74.95, 115.77, 117.35, 127.49, 127.87, 128.55, 137.39, 152.53, 153.01; IR (CHCl3): 3010, 2940, 2850, 1600, 1500, 1475, 1450, 1375, 1230, 1200, 1125, 1025, 925, 825 cm-1 ; Mass spectrum, m/z (rel.Intensity): 312(M+ 7), 212(15), 91(100), 71(5), 57(8), 43(10).

後処理

  1. customTo an argon-flushed flask
  2. additionwas added dropwise for 30 min
  3. stirringthe mixture was stirred for 1 h
  4. customThe solvent was then evaporated
  5. customthe residual crude product was triturated in a mixture of hexanes/ethyl acetate [70/30] for 1 h
  6. filtrationfiltered through a short silica gel pad
  7. customThe filtrate was evaporated
  8. customthe product was purified by flash chromatography on silica gel

出典と根拠

ORDレコード
ord-3827fd4d378a4d6ea3bb5eb2400e997c
出典データセット
uspto-grants-1997_08
特許番号
US05658493

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