Water → 2,3-Dihydro-1'-cyclopropylcarbonylspiro[benzofuran-2,4'-piperidine]
Reaction equation
[CH:1]1([C:4](Cl)=[O:5])[CH2:3][CH2:2]1.[NH:7]1[CH2:12][CH2:11][C:10]2([CH2:16][C:15]3[CH:17]=[CH:18][CH:19]=[CH:20][C:14]=3[O:13]2)[CH2:9][CH2:8]1.O.[OH-].[Na+]>N1C=CC=CC=1>[CH:1]1([C:4]([N:7]2[CH2:12][CH2:11][C:10]3([CH2:16][C:15]4[CH:17]=[CH:18][CH:19]=[CH:20][C:14]=4[O:13]3)[CH2:9][CH2:8]2)=[O:5])[CH2:3][CH2:2]1Participants
Procedure
1.8 g of cyclopropylcarbonyl chloride are added dropwise to a stirred solution at 0° C. of 3.2 g of 2,3-dihydrospiro[benzofuran-2,4'-piperidine] in 50 ml of pyridine. After total addition the reaction is stirred for 60 hours at ambient temperature and then heated at reflux for 3 hours. Thereafter, the reaction mixture is successively permitted to cool to ambient temperature, poured into 500 ml of water, basified with 20% sodium hydroxide and the solvent is removed under reduced pressure. The residue is triturated with 500 ml of water, extracted twice with ethyl acetate and the combined extracts are dried and the solvent is removed under reduced pressure, leaving a solid. The solid is recrystallized thrice from water to provide white flakes, 2,3-dihydro-1'-cyclopropylcarbonylspiro[benzofuran-2,4'-piperidine], mp 111°-113° C.
Workup
- additionAfter total addition the reaction
- temperatureheated
- temperatureat reflux for 3 hours
- temperatureto cool to ambient temperature
- customthe solvent is removed under reduced pressure
- customThe residue is triturated with 500 ml of water
- extractionextracted twice with ethyl acetate
- customthe combined extracts are dried
- customthe solvent is removed under reduced pressure
- customleaving a solid
- customThe solid is recrystallized thrice from water
Sources & evidence
- ORD record
- ord-ea94c57c3b624e278473202240485871
- Source dataset
- uspto-grants-1979_08
- Patent number
- US04166119
Reaction notes
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