HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 86736420, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | HCID 86736421 | HCID 86736421 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86736420 | HCID 86736420 | — |
Reaction Steps
(E)-α-(3,4,5-trimethoxyphenyl) ethylideneisopropylidene succinic anhydride (4 parts), prepared as in Example 3, in toluene (40 parts by volume), and aniline (1 part) were heated (12 hours) at 70°. Petrol was added and the liberated succinamic acid separated. The dry acid (1.8 parts) was dissolved in acetyl chloride (40 parts by volume) boiled for 2 hours and the solvent removed. Crystallization of the product from a toluene/petrol mixture gave (E)-α-(3,4,5-trimethoxyphenyl) ethylideneisopropylidene-N-phenylsuccinimide as pale yellow needles, melting point 169.5°. The compound shows similar photochromic properties to the corresponding (E)-anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04145536 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-16adddc280874970aa250c30f64e4969 |
| Source note | uspto-grants-1979_03 |