Cysteamine Hydrochloride → HCID 131718855, compound

HRID 54736Notes

Reaction equation

HRID 54736 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

HCID 9082Cysteamine HydrochlorideHCID 109207893,4,4-Trifluoro-3-butenoyl chloride

Product 1

HCID 131718855HCID 131718855, compoundYield 34%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

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

  1. temperatureis slowly heated
  2. temperatureto reflux for 15 min
  3. filtrationfiltered
  4. customThe product is recrystallized from absolute ethanol

Sources & evidence

ORD record
ord-37933f1a33a14ebf94302042b1b265ee
Source dataset
uspto-grants-1997_04
Patent number
US05623084

Reaction notes

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