HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N-(2-allyl-3-hydroxy-4-methylphenyl)-3,4,5,6-tetrahydrophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 2-Chloro-5-nitrophenol | HCID 69264 | — |
| Reactant | 2-Methyl-5-nitrophenol | HCID 93576 | — |
| Reactant | N-(2-allyl-4-chloro-3-hydroxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 57171405 | — |
| Product | N-(2-allyl-3-hydroxy-4-methylphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 57199273 | — |
Reaction Steps
N-(2-allyl-3-hydroxy-4-methylphenyl)-3,4,5,6-tetrahydrophthalimide (5A) was prepared, as yellow crystals, m.p.: 141°-143° C., from 2-methyl-5-nitrophenol and allyl bromide by the procedures described in Example 3 for preparing 3D from 2-chloro-5-nitrophenol and allyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05053071 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-1003bfc266a2469b9b83c5d074b97f6e |
| Source note | uspto-grants-1991_10 |