HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 1-(Aminomethyl)cycloheptanol hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1-(Aminomethyl)cycloheptan-1-ol | HCID 18438648 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Aminomethyl)cycloheptanol hydrochloride | HCID 18438647 | — |
Reaction Steps
Acetyl chloride (264 ml) and tetrahydrofuran (191 ml) were charged to a vessel containing 2-propanol (1143 ml) maintaining the temperature at 10° C. to 15° C. 1-(aminomethyl)cycloheptanol (381 g) in tetrahydrofuran (1613 ml) and tetrahydrofuran (381 ml) were charged maintaining the temperature at 10° C. to 15° C. The reaction mixture was stirred for 50 minutes and filtered. The filter cake was washed with premixed tetrahydrofuran/2-propanol [tetrahydrofuran (267 ml), 2-propanol (114 ml)], and tetrahydrofuran (1905 ml). The filter cake was dried at 40° C. for 23 hours to provide the title compound as a colourless solid (464 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106073B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d80c14b662184d83b836e9ce79c195cf |
| Source note | uspto-grants-2012_01 |