ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Methacryloyl chloride → 1-(2-Methylacryloyl)-L-proline

HRID 1249647
ノート
印刷プレビュー

反応式

HRID 1249647 の反応式
[NH:1]1[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4].C([O-])(O)=O.[Na+].[OH-].[Na+].[C:16](Cl)(=[O:20])[C:17]([CH3:19])=[CH2:18]>C(OCC)C.O>[C:16]([N:1]1[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4])(=[O:20])[C:17]([CH3:19])=[CH2:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 13528Methacryloyl chloride2 回HCID 14798Sodium Hydroxide2 回HCID 145742L-ProlineHCID 516892Sodium Bicarbonate

生成物 1

HCID 132083491-(2-Methylacryloyl)-L-proline

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

A mechanically stirred mixture of L-proline (42.0 grams, g), NaHCO3 (148 g), H2O (680 milliliters, ml) and diethyl ether (280 ml) was maintained in an ambient temperature bath at pH 10.5-10.7 (adjusted by the addition of concentrated aqueous NaOH), then treated portionwise over 20 minutes with a solution of redistilled methacryloyl chloride (40 ml) in diethyl ether (20 ml). Additional concentrated aqueous NaOH was added as needed to keep the pH at 10.5-10.7. Upon addition of all of the methacryloyl chloride (and pH stabilization), the mixture was stirred for 20 minutes at ambient temperature. The resulting immiscible phases were separated and the aqueous phase was extracted with two 250 ml portions of diethyl ether. The combined organic extracts were washed with H2O (50 ml), and the aqueous extract was added to the aqueous phase which phase was then acidified to pH 1 with concentrated aqueous HCl and then extracted with four 250 ml portions of ethyl acetate. The combined ethyl acetate extracts were washed with about 100 ml of brine (saturated aqueous sodium chloride solution) and then dried over Na2SO4. The resulting solution was filtered and concentrated in vacuo to about 230 ml and then heated to boiling, diluted with hexane (80 ml) and allowed to cool. Upon cooling, the desired N-methacryloyl-L-proline spontaneously crystallized as chunky white prisms (51.3 g). The concentrated mother liquor yielded a second crop of crystals (4.26 g) when crystallized as described above. A portion of the first crop was recrystallized twice from ethyl acetate to give an analytical sample, m.p. 102°-104.5° C., having the following spectral characteristics:

後処理

  1. customThe resulting immiscible phases were separated
  2. extractionthe aqueous phase was extracted with two 250 ml portions of diethyl ether
  3. washThe combined organic extracts were washed with H2O (50 ml)
  4. extractionthe aqueous extract
  5. additionwas added to the aqueous phase which phase
  6. extractionextracted with four 250 ml portions of ethyl acetate
  7. washThe combined ethyl acetate extracts were washed with about 100 ml of brine (saturated aqueous sodium chloride solution)
  8. dry with materialdried over Na2SO4
  9. filtrationThe resulting solution was filtered
  10. concentrationconcentrated in vacuo to about 230 ml
  11. temperatureheated
  12. additiondiluted with hexane (80 ml)
  13. temperatureto cool
  14. temperatureUpon cooling
  15. customthe desired N-methacryloyl-L-proline spontaneously crystallized as chunky white prisms (51.3 g)

出典と根拠

ORDレコード
ord-a1025c83f7fd4244af8db2b77f793178
出典データセット
uspto-grants-1986_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04633025

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート