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

HRID 621798
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HRID 621798 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 1004Phosphoric AcidHCID 6659Methyl 2-chloroacrylateHCID 83545Sarcosine methyl esterHCID 5360545Sodium

생성물 1

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

시약·촉매·용매 2

HCID 887Methanol용매3회
HCID 962
Water
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-8bad0a67092e48e791d3da720ceb7699
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04824958

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