Benzylamine → HCID 6931954, compound
Reaction equation
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:9]([C@H:11]1[O:13][CH2:12]1)[Cl:10]>>[CH2:1]([NH:8][CH2:12][C@H:11]([OH:13])[CH2:9][Cl:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
A scintillation vial was charged with benzylamine (1 g, 10 mmol), anhydrous petroleum ether (10 ml) and a stir bar. To this was added (S)-(+)-epichlorohydrin (0.925 g, 10 mmol) dropwise over a period of 20 min and the mixture was allowed to stir at room temperature. After 15 h, the white crystals precipitated from solution. These were collected by suction filtration, rinsed with cold petroleum ether (10 ml) and dried under vacuum to provide the title compound (1.0 g, 50%). Mass spectrum (ESI) 200.1 (M+1).
Workup
- customthe white crystals precipitated from solution
- filtrationThese were collected by suction filtration
- washrinsed with cold petroleum ether (10 ml)
- customdried under vacuum
Sources & evidence
- ORD record
- ord-49044c0758c443558a040f010852edb7
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08293721B2
Reaction notes
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