Triethylamine → 3-[(2-fluorophenyl)-acetyl]-4(R)-phenyl-2-oxazolidinone

HRID 566269

反応式

HRID 566269 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=O.[C:12]1([C@@H:18]2[CH2:22][O:21][C:20](=[O:23])[NH:19]2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C.C(Cl)(=O)C(C)(C)C>O.C1(C)C=CC=CC=1>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([N:19]1[C@H:18]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:22][O:21][C:20]1=[O:23])=[O:11]

参加物

7

反応物 4

HCID 8471TriethylamineHCID 62493Pivaloyl chloride2 回HCID 67979Benzeneacetic acid, 2-fluoro-HCID 730425(4R)-4-phenyl-1,3-oxazolidin-2-one

生成物 1

HCID 111506973-[(2-fluorophenyl)-acetyl]-4(R)-phenyl-2-oxazolidinone

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 1140Toluene溶媒

反応条件

温度
90 °C

実験手順

A mixture of 107.7 g of o-fluorophenylacetic acid, 100 g of (R)-4-phenyl-2-oxazolidinone, 186 g of triethylamine, and 1.0 L of toluene is heated to an internal temperature of 80° C. (heating mantle temperature 90° C.) to afford a solution; 88.5 g of pivaloyl chloride is added over period of 30 minutes with efficient stirring while maintaining an internal temperature 80-85° C. and stirred at this temperature for 2 hours. An additional 44.1 g of pivaloyl chloride is added over a period of 15 minutes while maintaining an internal temperature 80-85° C., and the mixture is stirred at the same temperature for additional 3 hours. The mixture is cooled to an internal temperature of 40° C. over a period of 10 minutes and 300 mL of water (prewarmed to 40° C.) is added over a period of 2 minutes while maintaining an internal temperature below 40-45° C. (slightly exothermic reaction). The organic layer is separated and washed with 358 mL of 2.17 N HCl solution (prewarmed to 40° C.) and 100 mL of water (prewarmed to 40° C.) sequentially while maintaining an internal temperature 40-45° C. and concentrated to dryness under reduced pressure (58-61 mbar; bath temperature, 51-53° C.) to obtain 3-[2-(2-fluorophenyl)-1-oxoethyl]-4-(R)-phenyl-2-oxazolidinone as a semi-solid. The semi-solid is suspended in 400 mL of tert-butyl methyl ether and the mixture is heated to reflux (internal temperature of 58-61° C.) to obtain a yellow solution. The solution is cooled to 20-25° C. over a period of 20 minutes and stirred at this temperture for 4 hours. The mixture is then further cooled to 5 to 9° C. and stirred at this temperature for additional 2 hours. The solids are collected by filtration and washed with a total of 27 mL of tert-butyl methyl ether (precooled to 5-9° C.) in three equal portions of 9 mL each. The product is dried at 45-50° C. (86-99 mbar) for 12 hours to obtain optically pure of 3-[2-(2-fluorophenyl)-1-oxoethyl]-4-(R)-phenyl-2-oxazolidinone as a white solid; m.p. 110-111° C.; [α]D: −110.4 (c=1, MeOH)

後処理

  1. customto afford a solution
  2. temperaturewhile maintaining an internal temperature 80-85° C.
  3. stirringstirred at this temperature for 2 hours
  4. temperaturewhile maintaining an internal temperature 80-85° C.
  5. stirringthe mixture is stirred at the same temperature for additional 3 hours
  6. temperatureThe mixture is cooled to an internal temperature of 40° C. over a period of 10 minutes
  7. temperaturewhile maintaining an internal temperature below 40-45° C. (
  8. customslightly exothermic reaction)
  9. customThe organic layer is separated
  10. washwashed with 358 mL of 2.17 N HCl solution (prewarmed to 40° C.) and 100 mL of water (prewarmed to 40° C.) sequentially
  11. temperaturewhile maintaining an internal temperature 40-45° C.
  12. concentrationconcentrated to dryness under reduced pressure (58-61 mbar; bath temperature, 51-53° C.)

出典と根拠

ORDレコード
ord-0eab56a2ffa340828aa3e3aa52a9bd64
出典データセット
uspto-grants-2001_01
特許番号
US06174888B1

関連ノート

読み込み中…