HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formamide → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | N-formyl-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethylamine | HCID 23292610 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | 1-[1-(3,4-Dichlorophenyl)cyclobutyl]ethylamine | HCID 13083140 | — |
Reaction Steps
The preparation of N-formyl-1-[1-(3,4-dichlorophenyl)cyclobutyl]ethylamine (m.p. 124°-125° C.) (Example 1(a) Formula I R1 =Me; R2 =H; R3 =H; R4 =CHO; R5 =4--Cl and R6 =3--Cl) described above was repeated and the product isolated by cooling the reaction mixture and collecting the solid produced by filtration. The formamide was then hydrolysed by concentrated hydrochloric acid in industrial methylated spirit to give the hydrochloride salt of 1-[1-(3,4-dichlorophenyl)cyclobutyl]ethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767790 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-484fc551f446422ab90c75b5447a20f6 |
| Source note | uspto-grants-1988_08 |