Formic Acid → 3-(Phthalimido)-propyl formate
Reaction equation
[C:1]1(=[O:15])[N:5]([CH2:6][CH2:7][CH2:8][OH:9])[C:4](=[O:10])[C:3]2=[CH:11][CH:12]=[CH:13][CH:14]=[C:2]12.[CH:16](O)=[O:17]>>[CH:16]([O:9][CH2:8][CH2:7][CH2:6][N:5]1[C:4](=[O:10])[C:3]2=[CH:11][CH:12]=[CH:13][CH:14]=[C:2]2[C:1]1=[O:15])=[O:17]Participants
3
Procedure
A mixture of 3-(phthalimido)-propanol (20.5 g) and formic acid (33 ml) was refluxed overnight and evaporated in vacuo to leave a yellow oil which crystallized from absolute ethanol to give colourless crystals with m.p. 68°-70° C.
Workup
- temperaturewas refluxed overnight
- customevaporated in vacuo
- customto leave a yellow oil which
- customcrystallized from absolute ethanol
- customto give colourless crystals with m.p. 68°-70° C.
Sources & evidence
- ORD record
- ord-106fdf697b954067947f319948b90715
- Source dataset
- uspto-grants-1988_03
- Patent number
- US04732998
Reaction notes
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