Hydrochloric Acid → HCID 59542561, compound
Reaction equation
C([O:3][C:4]([C:6]1[CH:10]=[C:9]([CH2:11][CH3:12])[S:8][CH:7]=1)=[O:5])C.[ClH:13]>[OH-].[Na+].C(O)C>[Cl:13][C:7]1[S:8][C:9]([CH2:11][CH3:12])=[CH:10][C:6]=1[C:4]([OH:3])=[O:5]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 140 °C
Procedure
5-Ethyl-thiophene-3-carboxylic acid ethyl ester (0.83 g, 3.8 mmol) was dissolved in a solution of aqueous sodium hydroxide (1 M, 6 mL) and ethanol (4 mL). The mixture was then heated to 140° C. for 10 minutes using microwave irradiation. The reaction mixture was acidified with 1 N hydrochloric acid and the resulting precipitate was isolated by filtration, washed with water and then dried under vacuum to give the title compound (0.53 g). 1H NMR (400 MHz, DMSO-d6): δ 7.05 (s, 1H), 2.75 (q, 2H), 1.4 (t, 3H), 1.2 (t, 3H).
Workup
- custommicrowave irradiation
- customthe resulting precipitate was isolated by filtration
- washwashed with water
- customdried under vacuum
Sources & evidence
- ORD record
- ord-eb0f1c4f528a4689a4cbc1885d7ca301
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08362008B2
Reaction notes
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