Methanol → HCID 23074222, compound
Reaction equation
[NH2:1][CH:2]([CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[C:3]([OH:5])=[O:4].S(Cl)([Cl:13])=O.[CH3:15]O>>[ClH:13].[NH2:1][CH:2]([CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[C:3]([O:5][CH3:15])=[O:4]Participants
4
Conditions
- Temperature
- 60 °C
Procedure
To a suspension of 2.18 g of 2-aminoheptanoic acid in 50 ml of methanol was dropwise added 2.19 g of thionyl chloride (manufactured by WAKO PURE CHEMICAL INDUSTRIES LTD.), and the mixture was stirred overnight at 60° C. Methanol and thionyl chloride were removed by evaporation and the residue was washed with 20 ml of ether to obtain 2.84 g of the title compound.
Workup
- customMethanol and thionyl chloride were removed by evaporation
- washthe residue was washed with 20 ml of ether
Sources & evidence
- ORD record
- ord-b71af3238fdf4d8a9ccdaeed5fd2d9e1
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07803792B2
Reaction notes
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