HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 11063236, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11063236 | HCID 11063236 | 60.4% |
Reaction Steps
Lithium (0.17 g, 24 mmol) was added in portions to a solution of benzonitrile (0.99 mL, 1.0 g, 9.7 mmol) and t-BuOH (0.93 mL, 0.72 g, 9.7 mmol) in NH3 (50 mL) and THF (10 mL) under N2 at −78° C. After 10 minutes, ethyl bromoacetate (2.2 mL, 3.3 g, 20 mmol) was added dropwise. After 1 hour, ammonium chloride (4.0 g, 75 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 (25 mL) was added, and the mixture extracted with EtOAc (3×25 mL). The combined organic extracts were washed with brine (50 mL), dried (MgSO4), and concentrated under reduced pressure. Flash chromatography (SiO2. CH2Cl2) afforded 1.12 g (60%) of product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294690B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-b65df186dda14a4498f867b99f61be1b |
| Source note | uspto-grants-2001_09 |