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1,3,5-Trioxane → (S)-4-Benzyl-3-((R)-2-hydroxymethyl-4-methylpentanoyl)oxazolidin-2-one

HRID 907200
ノート
印刷プレビュー

反応式

HRID 907200 の反応式
[CH2:1]([C@H:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:20])[CH2:15][CH2:16][CH:17]([CH3:19])[CH3:18])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCN(C(C)C)C(C)C.[O:30]1COCO[CH2:31]1>C(Cl)Cl.[Ti](Cl)(Cl)(Cl)Cl>[CH2:1]([C@H:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:20])[C@@H:15]([CH2:31][OH:30])[CH2:16][CH:17]([CH3:18])[CH3:19])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 80811,3,5-TrioxaneHCID 81531DiisopropylethylamineHCID 10869526(S)-4-Benzyl-3-(4-methylpentanoyl)oxazolidin-2-one

生成物 1

HCID 59556783(S)-4-Benzyl-3-((R)-2-hydroxymethyl-4-methylpentanoyl)oxazolidin-2-one収率 98.3%

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒2 回
HCID 6344
Dichloromethane
溶媒
4 回

反応条件

温度
0 °C

実験手順

Intermediate (2a) (14.5 g, 46.3 mmol) was dissolved in DCM (151 mL, 2.4 mol) and stirred at 0° C. under nitrogen. 1 M titanium tetrachloride in DCM (48.6 mL) was added and stirred for 15 minutes. DIPEA (8.9 mL, 51.0 mmol) was added dropwise at 0° C. and the mixture was stirred for 75 minutes. 1,3,5-Trioxane (4.6 g, 51.0 mmol) in DCM (30 mL) was then added. After 10 minutes a second equivalent of 1 M titanium tetrachloride in DCM (48.6 mL) was added and the mixture stirred at 0° C. for 5 hours. The reaction was then quenched with 250 mL of saturated ammonium chloride. Water and DCM were added, and the aqueous phase was extracted twice more with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated. The resulting material was purified by silica gel chromatography (0-60% EtOAc:hexanes) to provide intermediate (2b) (13.9 g).

後処理

  1. stirringstirred for 15 minutes
  2. stirringthe mixture was stirred for 75 minutes
  3. stirringthe mixture stirred at 0° C. for 5 hours
  4. customThe reaction was then quenched with 250 mL of saturated ammonium chloride
  5. additionWater and DCM were added
  6. extractionthe aqueous phase was extracted twice more with DCM
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe resulting material was purified by silica gel chromatography (0-60% EtOAc:hexanes)

出典と根拠

ORDレコード
ord-86923cba05d04a0eb093a44fe8749288
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08013005B2

反応ノート

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