HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 10900116, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10900116 | HCID 10900116 | 73% |
Reaction Steps
Lithium (1.73 g, 249 mmol) was added in portions to a stirred solution of benzonitrile (10.2 mL, 10.3 g, 99.9 mmol) and t-BuOH (9.6 mL, 7.4 g, 100 mmol) in NH3 (50 mL) and THF (10 mL) under N2 at −78° C. After stirring for 25 minutes, t-butyl bromoacetate (29.5 mL, 39.0 g, 200 mmol) was added dropwise. After 1 hour, ammonium chloride (41.8 g, 781 mmol) was added in portions. The reaction mixture was slowly warmed to room temperature while the NH3 was removed with a stream of N2. Water (125 mL) was added and the mixture extracted with MTBE (3×50 mL). The combined organic extracts were dried (MgSO4) and concentrated under reduced pressure. Flash chromatography (SiO2, CH2Cl2-1:14 MTBE:CH2Cl2) afforded 16.0 g (73%) of product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06538148B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-6360a34705194b6c85ffc04f6f9bf374 |
| Source note | uspto-grants-2003_03 |