Ethanol → HCID 131718307, compound
Reaction equation
[Cr:1].[S:2](=[O:6])(=[O:5])([OH:4])[OH:3].C(O)C.[S:10]([O-:14])([O-:13])(=[O:12])=[O:11].[NH2:15][C@H:16]([C:21]([OH:23])=[O:22])[CH2:17][CH2:18][S:19][CH3:20]>>[S:2]([O-:6])([O-:5])(=[O:4])=[O:3].[NH2:15][C@H:16]([C:21]([OH:23])=[O:22])[CH2:17][CH2:18][S:19][CH3:20].[Cr+3:1].[S:10]([O-:14])([O-:13])(=[O:12])=[O:11].[S:2]([O-:6])([O-:5])(=[O:4])=[O:3].[Cr+3:1]Participants
6
Procedure
Two grams of chromium plus 6 oxide (0.02 mol) is reacted with 0.03 moles of sulphuric acid in the presence of 0.04 moles of ethyl alcohol. The chromium plus 6 oxide is reduced to chromium plus 3 sulphate. The reaction mixture is heated and boiled until the solution turns green and no odor of acctaldehyde is given off. Thereafter 2.98 grams of L methionine is added and the mixture is heated on a steam bath until a dark green colored paste forms. The mixture is dried in a hot air oven and instrumental, and quantitative analysis as pre-viously described reveals the presence of a 1:1 L-form complex chromium methionine sulphate salt.
Workup
- temperatureThe reaction mixture is heated
- temperaturethe mixture is heated on a steam bath until a dark green colored paste forms
- customThe mixture is dried in a hot air oven
Sources & evidence
- ORD record
- ord-5621fd9587914c919efc5ead254ff16c
- Source dataset
- uspto-grants-1994_01
- Patent number
- US05278329
Reaction notes
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