HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 13853382, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13853382 | HCID 13853382 | — |
Reaction Steps
Ethyl p-aminobenzoate (7.3 g) was reacted with 37% formalin (formaldehyde in water) (3.2 ml), mercaptoacetic acid (3.0 ml) and xylene (300 ml). This reaction mixture was refluxed and the water formed thereby was removed azeotropically. After all the water was removed, xylene was evaporated under reduced pressure and the residual oil taken up in methylene chloride. Removal of the methylene chloride solvent left an orange solid which was recrystallized from ethanol to give ethyl 4-(4-oxo-3-thiazolidinyl)benzoate. This product had a melting point of 68°-69° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04664694 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-451403b1d9294175adc3d9a8587ff1ec |
| Source note | uspto-grants-1987_05 |