Diethyl Ether → HCID 86747411, compound
Reaction equation
[CH2:1]([NH2:4])[CH2:2][CH3:3].Br[CH:6]([CH3:12])[C:7]([O:9]CC)=[O:8].O(CC)[CH2:14][CH3:15]>>[CH2:14]([N:4]([CH2:1][CH2:2][CH3:3])[C@H:6]([C:7]([OH:9])=[O:8])[CH3:12])[CH3:15]Participants
4
Procedure
To a stirred solution of 11.8 parts of 1-propanamine in 24.9 parts of 1,1′-oxybis ethane there was added dropwise a solution of 18.1 parts of ethyl 2-bromopropanoate in 24.9 parts of 1,1′-oxybisethane. After stirring for 72 hours at room temperature, the reaction mixture was filtered and the filtrate was rinsed with 1,1′-oxybisethane. The combined 1,1′-oxybisethane layers were evaporated, yielding 15.9 parts (100%) of ethyl N-propylalanine as a residue (interm. 38).
Workup
- filtrationthe reaction mixture was filtered
- washthe filtrate was rinsed with 1,1′-oxybisethane
- customThe combined 1,1′-oxybisethane layers were evaporated
Sources & evidence
- ORD record
- ord-64804d1b8ef54be9899614b6a5087b10
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06201119B1
Reaction notes
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