1-Benzofuran-4-carboxylic acid → 2,3-Dihydro-1-benzofuran-4-carboxylic acid
Reaction equation
[O:1]1[C:5]2=[CH:6][CH:7]=[CH:8][C:9]([C:10]([OH:12])=[O:11])=[C:4]2[CH:3]=[CH:2]1>C(O)(=O)C.[Pd]>[O:1]1[C:5]2=[CH:6][CH:7]=[CH:8][C:9]([C:10]([OH:12])=[O:11])=[C:4]2[CH2:3][CH2:2]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
Benzofuran-4-carboxylic acid (10.0 g, 61.7 mmol) was hydrogenated (60 psi) in acetic acid (100 mL) over 10% Pd/C (2 g) for 12 hr. The mixture was filtered and the filtrate was diluted with water (500 mL) to give 2,3-dihydrobenzofuran-4-carboxylic acid as a white powder (8.4 g, 83%). A sample was recrystallized from isopropanol to give fine white needles (mp: 185.5°-187.5° C.).
Workup
- customfor 12 hr
- filtrationThe mixture was filtered
- additionthe filtrate was diluted with water (500 mL)
Sources & evidence
- ORD record
- ord-8789c4d41bc94e62b015a71ca0afbbce
- Source dataset
- uspto-grants-1999_01
- Patent number
- US05856529
Reaction notes
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