Allylamine → HCID 14093037, compound
Reaction equation
[CH2:1]([NH2:4])[CH:2]=[CH2:3].Cl[CH2:6][CH2:7][C:8]([OH:10])=[O:9]>>[CH2:1]([NH:4][CH2:6][CH2:7][C:8]([OH:10])=[O:9])[CH:2]=[CH2:3]Participants
3
Procedure
To a cooled solution of 125 mL aqueous allylamine (60%), 3-chloropropionic acid (20 g) was added portionwise while stirring over 5 minutes. The mixture was stirred at ambient temperature for 72 hours. The mixture was then evaporated to a viscous oily residue (40 g). The product consisted of a 1:1 mixture of 3-allylaminopropionic acid and allylamine hydrochloride. This product mixture was used without further purification for the preparation of the title compound in step 2.
Workup
- stirringThe mixture was stirred at ambient temperature for 72 hours
- customThe mixture was then evaporated to a viscous oily residue (40 g)
- additionThe product consisted of a 1:1 mixture of 3-allylaminopropionic acid and allylamine hydrochloride
- customThis product mixture was used without further purification for the preparation of the title compound in step 2
Sources & evidence
- ORD record
- ord-2ecb17d935214b2d958d921f99cb3ffa
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05807864
Reaction notes
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