HCID 67915250, compound → HCID 13100818, compound
Reaction equation
Cl.C([O:4][C:5](=[O:17])[CH2:6][NH:7][CH:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10][CH2:9]1)C>Cl>[CH:8]1([NH:7][CH2:6][C:5]([OH:17])=[O:4])[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10][CH2:9]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
N-(1-Indanyl)glycine ethyl ester hydrochloride (9.0 g) is dissolved in 100 ml of 5N hydrochloric acid, and the mixture is refluxed for 4 hours. The reaction mixture is concentrated to dryness under reduced pressure, 10 ml of water is added to the residue, and the mixture is neutralized with aqueous ammonia. The resulting crystalline precipitates are collected by filtration, washed with water, and dried, to give 6.0 g N-(1-indanyl)glycine as colorless needles. Melting point: 184°-186° C.
Workup
- temperaturethe mixture is refluxed for 4 hours
- concentrationThe reaction mixture is concentrated to dryness under reduced pressure, 10 ml of water
- additionis added to the residue
- customThe resulting crystalline precipitates
- filtrationare collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-989cb7eaba3d4fc2ac45d5e8f76345c4
- Source dataset
- uspto-grants-1985_06
- Patent number
- US04521607
Reaction notes
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