Hydrochloric Acid → 1383372-63-1
Reaction equation
[CH2:1]([C:8]1([OH:19])[CH2:11][N:10](C(OC(C)(C)C)=O)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:20]>>[ClH:20].[CH2:1]([C:8]1([OH:19])[CH2:11][NH:10][CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
tert-butyl 3-benzyl-3-hydroxyazetidine-1-carboxylate 3 (2.0 gm, 7.59 mmol) was taken into a round bottomed flask and was added methanolic-HCl (25 mL, 20%) and was stirred for 3 h at room temperature. After completion of the reaction (monitored by TLC), the solvent was removed under vacuum to get a white solid as a crude product. The crude product was washed with ethyl acetate repeatedly and then dried well to obtain compound 4 as a white solid (1.36 gm, 90%) which was used without further purification.
Workup
- customAfter completion of the reaction (monitored by TLC)
- customthe solvent was removed under vacuum
- customto get a white solid as a crude product
- washThe crude product was washed with ethyl acetate repeatedly
- customdried well
Sources & evidence
- ORD record
- ord-39e1016e19104652872b2cb2f596365e
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221792B2
Reaction notes
Loading…