Hydrochloric Acid → HCID 18551811, compound
Reaction equation
Cl.[CH2:2]([S:9][C:10]1[S:11][CH:12]([CH2:16][OH:17])[CH:13](O)[N:14]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(O)C>[CH2:2]([S:9][C:10]1[S:11][C:12]([CH2:16][OH:17])=[CH:13][N:14]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
0.2 ml of concentrated hydrochloric acid is added to 3.0 g of 2-benzylsulfanyl-5-hydroxymethyl-4,5-dihydrothiazol-4-ol in 25 ml of ethanol. The mixture is stirred at 50° C. for 12 hours, the solvent is removed in vacuo, and the residue is chromatographed on silica gel (ether:hexane; 1:1). The title compound is obtained in the form of a yellow oil (compound 3.1).
Workup
- customthe solvent is removed in vacuo
- customthe residue is chromatographed on silica gel (ether:hexane; 1:1)
Sources & evidence
- ORD record
- ord-c5ff8bb421c248809d0c3333e6399d37
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06548676B1
Reaction notes
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