HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[4-(Benzyloxy)anilino]-5-methoxybenzoic acid → HCID 13371473, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[4-(Benzyloxy)anilino]-5-methoxybenzoic acid | HCID 13371462 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Product | HCID 13371473 | HCID 13371473 | — |
Reaction Steps
1-[2-(4-Benzyloxyphenylamino)-5-methoxyphenyl]ethanone [XIII; R=5-CH3O, OR°=4-OCH2C6H5, R"=H] was prepared by reduction of 2-(4-benzyloxyphenylamino)-5-methoxybenzoic acid (Example 1A, part a) with methyllithium according to the procedure of Example 5, part (a), and obtained in the form of a yellow-orange powder, m.p. 80°-81.5° C. when recrystallized from toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496590 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-9794b4ef7f5a48b99c2836d4e036868a |
| Source note | uspto-grants-1985_01 |