HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 5-Methyl-4-(dimethylaminomethyl)-2-thiophenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N,N,2-Trimethyl-3-thiophenemethanamine | HCID 10374728 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 5-Methyl-4-(dimethylaminomethyl)-2-thiophenemethanol | HCID 12926526 | — |
Reaction Steps
A mixture of N,N,2-trimethyl-3-thiophenemethanamine (6.1 g), paraformaldehyde (3.0 g) in conc. hydrochloric acid (20 ml) and acetic acid (45 ml) was stirred at 0° to 5° C. for 1 hour, and at 8° for 72 hours. The mixture was added to an ice-cold, saturated solution of sodium carbonate. Aqueous 5M sodium hydroxide was added and the mixture was stirred for 20 hours. The solution was extracted with chloroform and the organic extract was washed with dilute sodium hydroxide and saturated brine, dried and evaporated to leave an oil. This residue was distilled to give the title compound (6 g) as a pale yellow oil b.p. 120°/0.1 mm. The oxalate salt was formed in ethanol and ethyl acetate m.p. 129°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04777179 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-0a8734c2cff74e8e88755fef2ed11c15 |
| Source note | uspto-grants-1988_10 |