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Trifluoroacetic acid → Methyl 3-((di-tert-butoxyphosphoryloxy)methyl)benzoate

HRID 595036
ノート
印刷プレビュー

反応式

HRID 595036 の反応式
Br[CH2:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7].[C:13]([O:17][P:18]([O-:25])([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])([CH3:16])([CH3:15])[CH3:14].C([N+](CCCC)(CCCC)CCCC)CCC.O.CO.C(O)(C(F)(F)F)=O>CN(C=O)C.CCOCC>[C:21]([O:20][P:18]([O:25][CH2:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7])([O:17][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:19])([CH3:24])([CH3:23])[CH3:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6422Trifluoroacetic acidHCID 517981Methyl 3-(bromomethyl)benzoateHCID 22242641Methanol--water (1/1)HCID 22339116Tetra-n-butylammonium di-tert-butylphosphate

生成物 1

HCID 68385353Methyl 3-((di-tert-butoxyphosphoryloxy)methyl)benzoate

試薬・触媒・溶媒 2

HCID 3283
Diethyl Ether
溶媒
HCID 6228Dimethylformamide溶媒

実験手順

To a stirred mixture of methyl 3-(bromomethyl)benzoate (1.08 g, 4.71 mmol) in DMF (20 mL) was added tetrabutylammonium di-tert-butyl phosphate (2.34 g, 5.19 mmol). The mixture was stirred at room temperature for 1.5 h, then diluted with ether and washed sequentially with 10% LiCl solution and brine. The organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated. The crude material was purified by flash chromatography (Teledyne ISCO CombiFlash 0% to 100% solvent A/B=hexane/EtOAc, REDISEP® SiO2 40 g, detecting at 254 nM, and monitoring at 220 nM). Concentration of appropriate fractions provided Preparation 46A (1.38 g, 82%): HPLC: RT=3.163 min (H2O/MeOH with TFA, CHROMOLITH® ODS, 4.6×50 mm, gradient=4 min, wavelength=220 nm); MS(ES): m/z=359 [M+H+]; 1H NMR (400 MHz, DMSO-d6) δ 8.01 (s, 1H), 7.94-7.89 (m, 1H), 7.66 (d, J=7.9 Hz, 1H), 7.58-7.48 (m, 1H), 5.01 (d, J=8.4 Hz, 2H), 3.86 (s, 3H), 1.41 (s, 18H).

後処理

  1. washwashed sequentially with 10% LiCl solution and brine
  2. dry with materialThe organic layers were dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe crude material was purified by flash chromatography (Teledyne ISCO CombiFlash 0% to 100% solvent A/B=hexane/EtOAc, REDISEP® SiO2 40 g
  6. customConcentration of appropriate fractions provided

出典と根拠

ORDレコード
ord-0c77a5f264e5447395c4de062696abda
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242941B2

反応ノート

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