HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-Amino-1,1,1-trifluoro-2-methyl-2-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 19347508 | HCID 19347508 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | 4-Amino-1,1,1-trifluoro-2-methyl-2-butanol | HCID 79006473 | 81% |
Reaction Steps
A 1.0M solution of lithium aluminium hydride in tetrahydrofuran (30 ml, 30.0 mmol) was added dropwise to a solution of 4,4,4,-trifluoro-3-hydroxy-3-methyl butyramide (1.77 g, 10 mmol). The reaction was stirred at room temperature for 20 h, then quenched with water (1.2 ml), then 4M aqueous sodium hydroxide (1.2 ml), then water (3.6 ml). The inorganic salts were filtered off and the filtrate evaporated to dryness to yield 4-amino-1,1,1-trifluoro-2-methylbutan-2-ol (1.27 g, 81%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07671080B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-0ce0c2b5b6994051960131f4d74d0e48 |
| Source note | uspto-grants-2010_03 |