HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → N-Benzyloxyphthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Product | N-Benzyloxyphthalimide | HCID 255292 | 64% |
Reaction Steps
The title compound was prepared from 2-hydroxyisoindoline-1,3-dione and (bromomethyl)benzene in 64% yield using the same procedure as described in the synthesis of intermediate G. LCMS (method A): [MH]+=254, tR=5.19 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507676B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-8bf1f8d9157046c999620e38ee1a0e33 |
| Source note | uspto-grants-2013_08 |