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Phosphoric Acid → Methyl 3-hydroxy-1-methyl-1H-pyrrole-2-carboxylate

HRID 621798
ノート
印刷プレビュー

反応式

HRID 621798 の反応式
[NH:1]([CH2:3][C:4](OC)=O)[CH3:2].Cl[C:9](=[CH2:14])[C:10]([O:12][CH3:13])=[O:11].[Na].[OH:16]P(O)(O)=O>CO.O>[OH:16][C:14]1[CH:4]=[CH:3][N:1]([CH3:2])[C:9]=1[C:10]([O:12][CH3:13])=[O:11]
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 1004Phosphoric AcidHCID 6659Methyl 2-chloroacrylateHCID 83545Sarcosine methyl esterHCID 5360545Sodium

生成物 1

HCID 54697147Methyl 3-hydroxy-1-methyl-1H-pyrrole-2-carboxylate

試薬・触媒・溶媒 2

HCID 887Methanol溶媒3 回
HCID 962
Water
溶媒

実験手順

Methyl sarcosinate (14.5 g, 0.14 moles) is added dropwise to methyl α-chloroacrylate (16.9 g, 0.14 moles), stirred and cooled in an ice bath. After 15 minutes the mixture is dissolved in methanol (30 mL) and added dropwise to a solution of sodium (9.7 g, 0.42 moles) in methanol (125 mL) under argon. After 18 hours at room temperature, the mixture is striped of methanol under reduced pressure. The residue is taken up in water (300 mL), acidified with H3PO4, and extracted with ethyl acetate (5×100 mL). The combined extracts are dried over MgSO4, concentrated under reduced pressure and filtered through a short column of silica gel. The filtrate is stripped of solvent under reduced pressure, leaving the product (16.5 g) as an oil sufficiently pure for further use. An analytically pure sample was obtained by vacuum distillation; bp 61°-64° C. (0.5 mm) followed by recrystallization of the distillate from n-pentane to afford the product as shiny white crystals; mp 44°-46° C.

後処理

  1. temperaturecooled in an ice bath
  2. extractionextracted with ethyl acetate (5×100 mL)
  3. dry with materialThe combined extracts are dried over MgSO4
  4. concentrationconcentrated under reduced pressure
  5. filtrationfiltered through a short column of silica gel

出典と根拠

ORDレコード
ord-8bad0a67092e48e791d3da720ceb7699
出典データセット
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04824958

反応ノート

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