HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Propanone, 1-(3,4-dimethoxyphenyl)- → (+-)-3,4-Dimethoxyamphetamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Propanone, 1-(3,4-dimethoxyphenyl)- | HCID 69896 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (+-)-3,4-Dimethoxyamphetamine | HCID 8423 | 99.5% |
Reaction Steps
To 2 g (10.29 mmol) of 3,4-dimethoxyphenyl acetone was added 10 mL of methanol, 7.9 g (102 mmol) of ammonium acetate, 844 mg (10.2 mmol) of sodium acetate and 970 mg (15.4 mmol) of sodium cyanoborohydride. The pH of the reaction was adjusted to between 6-7 by addition of glacial acetic acid. The reaction mixture was allowed to stir at room temperature 18 hours and concentrated under reduced pressure. To the residue 100 mL of water was added, and the pH of the reaction was adjusted to 14 using 6 N NaOH. The aqueous layer was extracted with 6×30 mL of chloroform. Organic layers were combined, dried (Na2SO4) and concentrated under reduced pressure to give 2 g (10.24 mmol, 99%) of 3A as a light yellow gum (M+H, 196).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060847B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-338c120e9bf24a03a3e39a3ea9bce53c |
| Source note | uspto-grants-2006_06 |