Water → Benzyl 5-formyl-1H-pyrrole-2-carboxylate

HRID 2384084Notes

Reaction equation

HRID 2384084 reaction equation
[CH2:1]([O:8][C:9]([C:11]1[NH:12][CH:13]=[CH:14][CH:15]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN([CH:19]=[O:20])C.P(Cl)(Cl)(Cl)=O.O>ClCCCl>[CH2:1]([O:8][C:9]([C:11]1[NH:12][C:13]([CH:19]=[O:20])=[CH:14][CH:15]=1)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Conditions

Temperature
50 °C

Procedure

Next, To a stirred solution of 1H-pyrrole-2-carboxylic acid benzylester (2.0 g, 9.94 mmol) in 1,2-dichloroethane (15 mL) at 5° C. is sequentially added DMF (1.12 g, 15.31 mmol) and phosphoryl trichloride (2.35 g, 15.31 mmol). After the addition, the mixture is heated to 50° C. and stirred for an hour. Water is added and the mixture is extracted with ethyl acetate (3×). The combined organic layers are washed with water and brine then is dried over magnesium sulfate. The solvent is removed under reduced pressure and the residue is purified by flash chromatography (heptane/ethyl acetate=3:1) to give 5-formyl-1H-pyrrole-2-carboxylic acid benzyl ester; HPLC Retention time 1.64 minutes (condition C): MS 230.3 (M+1).

Workup

  1. customat 5° C.
  2. additionAfter the addition
  3. extractionthe mixture is extracted with ethyl acetate (3×)
  4. washThe combined organic layers are washed with water and brine
  5. dry with materialthen is dried over magnesium sulfate
  6. customThe solvent is removed under reduced pressure
  7. customthe residue is purified by flash chromatography (heptane/ethyl acetate=3:1)

Sources & evidence

ORD record
ord-d9ce61be20174d5abfe8f9b432080d9a
Source dataset
uspto-grants-2012_09
Patent number
US08263629B2

Reaction notes

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