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Chlorotrimethylsilane → N-(Triphenylmethyl)-D-serine

HRID 389379
ノート
印刷プレビュー

反応式

HRID 389379 の反応式
[NH2:1][C@@H:2]([C:5]([OH:7])=[O:6])[CH2:3][OH:4].C[Si](Cl)(C)C.C[Si](C)(C)N[Si](C)(C)C.[C:22](Cl)([C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1)([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>ClCCl.CO.C(N(CC)CC)C>[C:22]([NH:1][C@@H:2]([C:5]([OH:7])=[O:6])[CH2:3][OH:4])([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)([C:35]1[CH:36]=[CH:37][CH:38]=[CH:39][CH:40]=1)[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=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

8

反応物 4

HCID 6397ChlorotrimethylsilaneHCID 6456Trityl chlorideHCID 13838HexamethyldisilazaneHCID 71077D-Serine

生成物 1

HCID 12042811N-(Triphenylmethyl)-D-serine

試薬・触媒・溶媒 3

HCID 887Methanol溶媒2 回
HCID 6344
Dichloromethane
溶媒
2 回
HCID 8471Triethylamine溶媒

反応条件

温度
0 °C

実験手順

To dichloromethane (400 ml), D-serine (50 g) was added at ambient temperature under nitrogen atmosphere to form a suspension and then trimethylsilyl chloride (61.92 g) and hexamethyldisilazane (107.5 ml) were added to the suspension in 10-15 minutes at ambient temperature. The reaction mixture was refluxed at 35° C. to 40° C. for 3 hours and then it was cooled to 0° C. To this mixture, a solution of anhydrous methanol (22.83 g) in dichloromethane (50 ml) was added at 0° C. and the mixture was allowed to reach at room temperature. Triethylamine (48.14 g) was slowly added to it at 25° C. to 30° C. and then trityl chloride (132.63 g) was added in 3 lots to the mixture at an interval of 10 minutes. The reaction mixture was then stirred for overnight under nitrogen at ambient temperature. After completion of the reaction, methanol (76.12 g) was added at ambient temperature in 10-15 minutes and the solvent was recovered under vacuum at 40° C. to 45° C. Hexane (400 ml) and 5% citric acid solution (750 ml) was added to the recovered solid and filtered. The solid product obtained was washed with water (750 ml) and hexanes (200 ml) and then filtered. The filtered solid was washed with hexanes (200 ml) and dried to obtain the titled product. Yield=125 gm.

後処理

  1. customto form a suspension
  2. temperatureThe reaction mixture was refluxed at 35° C. to 40° C. for 3 hours
  3. customto reach at room temperature
  4. additionwas added at ambient temperature in 10-15 minutes
  5. customthe solvent was recovered under vacuum at 40° C. to 45° C
  6. additionHexane (400 ml) and 5% citric acid solution (750 ml) was added to the recovered solid
  7. filtrationfiltered
  8. customThe solid product obtained
  9. washwas washed with water (750 ml) and hexanes (200 ml)
  10. filtrationfiltered
  11. washThe filtered solid was washed with hexanes (200 ml)
  12. customdried

出典と根拠

ORDレコード
ord-0155b6584a4a4ce69859e595d627fbb6
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08378142B2

反応ノート

読み込み中…

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