Potassium Hydroxide → HCID 12926018, compound
Reaction equation
C([NH:4][C:5]1[CH:6]=[CH:7][C:8]2[C:14](=[O:15])[C:11]3([CH2:13][CH2:12]3)[O:10][C:9]=2[CH:16]=1)(=O)C.[OH-].[K+]>CO>[NH2:4][C:5]1[CH:6]=[CH:7][C:8]2[C:14](=[O:15])[C:11]3([CH2:13][CH2:12]3)[O:10][C:9]=2[CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 1.09 g. of 6-acetylaminospiro[benzo[b]furan-2(3H),1'-cyclopropane]-3-one in 50 ml. of methanol was added 0.8 g. of potassium hydroxide, and the mixture was refluxed for 0.5 hour. The solvent was evaporated off under reduced pressure. To the residue was added water, and the precipitating crystals were collected by filtration, washed with water and dried. The crystals were recrystallized from methanol to obtain 6-aminospiro[benzo[b]furan-2(3H),1'-cyclopropane]-3-one as colorless prisms melting at 188°-189° C.
Workup
- customThe solvent was evaporated off under reduced pressure
- additionTo the residue was added water
- filtrationthe precipitating crystals were collected by filtration
- washwashed with water
- customdried
- customThe crystals were recrystallized from methanol
Sources & evidence
- ORD record
- ord-e5a8400be145407aae414a761284ea26
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04284644
Reaction notes
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