HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 70419362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Reactant | 2-(4-Acetyl-2,3-dichlorophenoxy)acetic acid | HCID 12328188 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70419362 | HCID 70419362 | — |
Reaction Steps
(2,3-Dichloro-4-acetylphenoxy)acetic acid (U.S. Pat. No. 3,453,312) (7.89 g, 0.03 mole), dimethylamine hydrochoride (2.34 g, 0.03 mole), paraformaldehyde (1.05 g, 0.033 mol. equiv.) and glacial acetic (1 ml) were combined and heated on a steam bath for two hours. The reaction mixture was treated with hot ethanol (50 ml) and then cooled. The white solid was separated by filtration, washed with ethanol, dried and recrystallized from a mixture of ethanol and ether to give [2,3-dichloro-4-(3-dimethylaminopropionyl)phenoxy]acetic acid hydrochloride, m.p. 194°-196° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04719310 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-f9e1dd39198e492fb3854a4e2c079966 |
| Source note | uspto-grants-1988_01 |