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Acetic Anhydride → N-Acetyl-D-serine

HRID 1401873
ノート
印刷プレビュー

反応式

HRID 1401873 の反応式
[C:1](OC(=O)C)(=[O:3])[CH3:2].[NH2:8][C@H:9]([CH2:13][OH:14])[C:10]([OH:12])=[O:11]>C(O)(=O)C>[C:1]([NH:8][C@H:9]([CH2:13][OH:14])[C:10]([OH:12])=[O:11])(=[O:3])[CH3:2]
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

4

反応物 2

HCID 7918Acetic AnhydrideHCID 71077D-Serine

生成物 1

HCID 10844522N-Acetyl-D-serine

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒2 回

反応条件

温度
32.5 °C

実験手順

Acetic anhydride (23.4 ml) was added to the suspension of (R)-2-amino-3-hydroxypropanoic acid compound of formula-3 (20 grams) in acetic acid (300 ml) and stirred for 24 hours at 30-35° C. After completion of the reaction, acetic acid was removed by distillation followed by co-distillation with tetrahydrofuran. Isopropyl alcohol (60 ml) and methyltertiarybutylether (120 ml) was added to the obtained residue and stirred for 30 minutes. The obtained solid was filtered off and then solvent from the filtrate was distilled off completely under reduced pressure to get the title compound.

後処理

  1. customwas removed by distillation
  2. additionIsopropyl alcohol (60 ml) and methyltertiarybutylether (120 ml) was added to the obtained residue
  3. stirringstirred for 30 minutes
  4. filtrationThe obtained solid was filtered off
  5. distillationsolvent from the filtrate was distilled off completely under reduced pressure

出典と根拠

ORDレコード
ord-1527d0c2ec9c4fb6a7de60d6d9135503
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08907132B2

反応ノート

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