HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl bromoacetate → DI-T-Butyl iminodiacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | L-tert-Leucine | HCID 164608 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | DI-T-Butyl iminodiacetate | HCID 4393691 | 67.2% |
Reaction Steps
To a solution of t-butylglycine (1.40 g, 10.67 mmol) in acetonitrile (20 mL) cooled to 0° C. was added ethyldisopropylamine (1.86 mL, 10.67 mmol) and t-butyl bromoacetate (1.57 mL, 10.67 mmol). The resulting solution was stirred for 24 h at room temperature. The mixture was concentrated to dryness in vacuo, water was added and the solution was extracted with dichloromethane (3×70 mL). The combined organic phases were washed with brine (70 mL), dried over Na2SO4 and concentrated to dryness in vacuo. The crude material was purified by silica gel chromatography (20-80% EtOAc in hexanes) to give the compound 14 (0.88 g, 33.6%). 1H NMR (400 MHz, CDCl3) δ 1.43 (s, 18H), 3.30 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901072B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-198517d0fac94c42853f8dbcc2e369df |
| Source note | uspto-grants-2014_12 |