Sodium Hydroxide → HCID 13882821, compound
Reaction equation
[S:1]1[C:5]([CH2:6][CH:7]2[CH2:16][CH2:15][C:14]3[CH:13]=[C:12]([C:17]([O:19]CC)=[O:18])[CH:11]=[CH:10][C:9]=3[CH2:8]2)=[CH:4][N:3]=[CH:2]1.[OH-].[Na+]>CO>[S:1]1[C:5]([CH2:6][CH:7]2[CH2:16][CH2:15][C:14]3[CH:13]=[C:12]([C:17]([OH:19])=[O:18])[CH:11]=[CH:10][C:9]=3[CH2:8]2)=[CH:4][N:3]=[CH:2]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3.92 g of ethyl 6-(5-thiazolylmethyl)-5,6,7,8-tetrahydro-2-naphthalenecarboxylate was added to a mixture of 10 ml of a 10% aqueous solution of sodium hydroxide and 30 ml of methanol and the mixture was heated under reflux for 1 hour. The reaction mixture was concentrated to dryness in vacuo and the residue was dissolved in water. A small amount of insoluble material was removed by filtration and the filtrate was adjusted to pH 6 with hydrochloric acid. The precipitate formed was collected by filtration to give 2.71 g of 6-(5-thiazolylmethyl)-5,6,7,8-tetrahydro-2-naphthalenecarboxylic acid as a powder. The powder was suspended in 20 ml of water and 0.42 g of sodium hydroxide was added thereto. The insoluble material was removed by filtration and the filtrate was concentrated in vacuo. The residue was recrystallized from a mixture of ethanol and diethyl ether to give 1.92 g of sodium carboxylate of the above product as a colorless powder with m.p. above 280° C.
Workup
- temperaturethe mixture was heated
- temperatureunder reflux for 1 hour
- concentrationThe reaction mixture was concentrated to dryness in vacuo
- dissolutionthe residue was dissolved in water
- customA small amount of insoluble material was removed by filtration
- customThe precipitate formed
- filtrationwas collected by filtration
Sources & evidence
- ORD record
- ord-0f7f6fa0f8ca4c748e1e4e109f498b92
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04777257
Reaction notes
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