HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4,4,4-trifluoro-2-hydroxybutanoate → 4,4,4-Trifluoro-2-hydroxybutanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4,4,4-trifluoro-2-hydroxybutanoate | HCID 21600538 | — |
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Product | 4,4,4-Trifluoro-2-hydroxybutanamide | HCID 90157102 | — |
Reaction Steps
A solution of 12-3 (200 mg, 1.16 mmol) in 7N NH3/MeOH (10 mL) was heated at 70° C. overnight. The reaction mixture was filtered, and the filtrate was concentrated to dryness. The residue was dissolved in 1,2-dimethoxyethane (10 mL) and filtered to remove insolubles. The filtrate was concentrated to dryness to afford Intermediate 12. 1H NMR (500 MHz, DMSO-d6) δ 7.40 (br s, 1H), 7.34 (br s, 1H), 5.93 (m, 1H), 4.10 (m, 1H), 2.64-2.65 (m, 1H), 2.40-2.41 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428492B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-20dbfbff0a8c4a75b6880e7ff4c3a084 |
| Source note | uspto-grants-2016_08 |