Hydrochloric Acid → HCID 90370160, compound
Reaction equation
[N:1]1([CH2:7][C:8]2[S:12][C:11]([C:13]([O:15]C)=[O:14])=[CH:10][CH:9]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[ClH:17]>>[ClH:17].[N:1]1([CH2:7][C:8]2[S:12][C:11]([C:13]([OH:15])=[O:14])=[CH:10][CH:9]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
A mixture of 3.01 g of methyl 5-(morpholin-4-ylmethyl)thiophene-2-carboxylate and 30 mL of 6.0 M hydrochloric acid was subjected to heating under reflux overnight at 100° C. The reaction mixture was concentrated under reduced pressure, and the residue was washed with acetonitrile, thereby obtaining 3.05 g of 5-(morpholin-4-ylmethyl)thiophene-2-carboxylic acid hydrochloride.
Workup
- temperatureto heating
- concentrationThe reaction mixture was concentrated under reduced pressure
- washthe residue was washed with acetonitrile
Sources & evidence
- ORD record
- ord-ae05f8f1a2144a68a9954a6788c5b044
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062032B2
Reaction notes
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