HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(cyclopentyloxy)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(cyclopentyloxy)-1H-isoindole-1,3(2H)-dione | HCID 10263287 | 49.2% |
Reaction Steps
A mixture of bromocyclopentane (14.9 g), N-hydroxyphthalimide (16.3 g), triethylamine (15 ml), and dimethylformamide (30 ml) was stirred for 16 hours, then poured into water (500 ml). The oily mixture was extracted with ethyl acetate, and the combined extracts, after washing (water), drying, and removal of solvent gave a white solid. This solid was recrystallised from ethanol to give N-cyclopentyloxyphthalimide (11.37 g, 49%); m.p. 81.2°-82.5°; νmax. (CHBr3) include 1780, 1720 cm-1 (CO--N--CO), 970 cm-1 (>N--O--<CH); τ values (DMSO-d6) 2.08 (4 Ar-H), 5.12 (cyclopentyl 1-H), 8.18 (4-CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04033950 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-2f32ca15da8549069242d04abc088488 |
| Source note | uspto-grants-1977_07 |