Cysteamine Hydrochloride → HCID 131718855, compound
Reaction equation
[F:1][C:2](=[C:7]([F:9])[F:8])[CH2:3][C:4]([Cl:6])=[O:5].Cl.[NH2:11][CH2:12][CH2:13][SH:14]>CCOCC>[ClH:6].[F:1][C:2](=[C:7]([F:9])[F:8])[CH2:3][C:4](=[O:5])[S:14][CH2:13][CH2:12][NH2:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3,4,4-trifluoro-3-butenoyl chloride (2.5 g, 0.0158 mole) and 2-aminoethanethiol hydrochloride (1.14 g, 0.010 mole) is slowly heated to reflux for 15 min. The mixture is cooled to room temperature and treated with dry ether and filtered. The product is recrystallized from absolute ethanol to give 0.8 g of the title compound as a off-white solid, a 34% yield. m.p. 95°-115° C.
Workup
- temperatureis slowly heated
- temperatureto reflux for 15 min
- filtrationfiltered
- customThe product is recrystallized from absolute ethanol
Sources & evidence
- ORD record
- ord-f06e305f991b448399fea331e0aaa0b4
- Source dataset
- uspto-grants-1996_10
- Patent number
- US05561162
Reaction notes
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