Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Clenbuterol | HCID 2783 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 70405389 | HCID 70405389 | — |
Reaction Steps
A mixture containing 2.5 g of 4-amino-α-[(tert-butylamino)methyl]-3,5-dichlorobenzyl alcohol, 25 ml of pyridine and 10 ml of acetic anhydride is stirred for three hours and evaporated to dryness in vacuo with heating up to 70° C. The residue is treated with ice, 100 ml of CH2Cl2 and 50 ml of 10% NaOH solution. The CH2Cl2 phase is separated, and the aqueous portion is further extracted with CH2CL2 (2×50 ml). The combined CH2CL2 solutions are dried (Na2SO4) and evaporated to dryness to afford a solid after scratching. The solid is washed with hexane and collected to afford 2.61 g of the title compound, mp 126°-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04404222 |
|---|
| Source dataset | uspto-grants-1983_09 |
|---|
| ORD ID | ord-d8c82e9b16624c6f8361bebf94b2c35e |
|---|
| Source note | uspto-grants-1983_09 |
|---|