Methyl chloroformate → 4-Fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonate

HRID 404595

反応式

HRID 404595 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([C:9]2([CH3:15])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)[CH:3]=1.Cl[C:17]([O:19][CH3:20])=[O:18]>CN(C1C=CN=CC=1)C.C(Cl)Cl>[C:17](=[O:18])([O:19][CH3:20])[O:8][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][C:4]=1[C:9]1([CH3:15])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1

参加物

5

反応物 2

HCID 6586Methyl chloroformateHCID 593949974-Fluoro-2-(1-methylcyclohexyl)phenol

生成物 1

HCID 593950614-Fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonate収率 72.1%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane溶媒

実験手順

To a solution of 4-fluoro-2-(1-methylcyclohexyl)phenol (23.5 g, 113 mmol), TEA (31 mL, 226 mmol) and DMAP (700 mg, 5.7 mmol) in CH2Cl2 (250 mL) was added methyl chloroformate dropwise at 0° C. The mixture was allowed to warm to room temperature and stirred for 2 hours. The reaction mixture was poured onto crushed ice and extracted with CH2Cl2 (100 mL×3). The organic layer was washed with brine, dried over MgSO4, evaporated under vacuum. The crude product was purified by chromatography on silica gel diluted with (hexane:ethyl acetate=100:1) to give 4-fluoro-2-(1-methylcyclohexyl)phenyl methyl carbonate as red brown oil (43.9 g, 72.1% yield). 1H NMR (400 MHz, CDCl3) δ 7.10 (dd, J=3.2, 11.2 Hz, 1H), 7.05-7.02 (m, 1H), 6.93-6.88 (m, 1H), 3.91 (s, 3H), 2.02-1.96 (m, 2H), 1.66-1.36 (m, 8H), 1.23 (s, 3H).

後処理

  1. additionThe reaction mixture was poured
  2. customonto crushed ice
  3. extractionextracted with CH2Cl2 (100 mL×3)
  4. washThe organic layer was washed with brine
  5. dry with materialdried over MgSO4
  6. customevaporated under vacuum
  7. customThe crude product was purified by chromatography on silica gel
  8. additiondiluted with (hexane:ethyl acetate=100:1)

出典と根拠

ORDレコード
ord-9409f5309d474ff5ad56ae7eb7f8bc9f
出典データセット
uspto-grants-2014_06
特許番号
US08748612B2

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