HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 3-Allyloxycarbonyl-5-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 5-Nitroisophthalic acid | HCID 12069 | — |
| Product | 3-Allyloxycarbonyl-5-nitrobenzoic acid | HCID 20655860 | — |
Reaction Steps
5-Nitroisophthalic acid (5 g) was converted to the mono allyl ester using one equivalent of allyl bromide (2 ml) using a similar method to that described in example 1. The requited acid (2.7 g) was extracted from the organic phase with aqueous NaHCO3. The organic layer contained the di-allyl ester (2.7 g). The mono acid, 3-allyloxycarbonyl-5-nitrobenzoic acid, was obtained as a white solid. Nmr (CDCl3): 4.87 (d, 2H); 5.3-5.5 (q, 2H); 5.97-6.15 (m, 1H); 9.01 (t, 3H.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07342005B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-1e346626875841b6bd6e0db1fbb8cc5a |
| Source note | uspto-grants-2008_03 |