HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 15582850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hexahydrophthalic anhydride | HCID 85689 | — |
| Reactant | HCID 15582849 | HCID 15582849 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15582850 | HCID 15582850 | — |
Reaction Steps
A mixture of 2.88 g. of 1.52 g. of cyclohexane-1,2-dicarboxylic anhydride 2.88 g. of 4-bromo-3-(1-ethoxycarbonylethyloxy)aniline (nD25 =1.5590) and 10 ml. of acetic acid was refluxed with stirring for 2 hours and the reaction mixture was cooled to room temperature and water was added. The precipitate was separated by a filtration and was recrystallized from a mixture of benzene-cyclohexane to obtain 3.89 g. of Compound No. 18 shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536209 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-2afdfcc1a5d44e37aa10adc59fcffcdb |
| Source note | uspto-grants-1985_08 |