HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Tert-butyl 2-acetamido-1-(4-chlorophenyl)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-butyl N-[2-amino-1-(4-chlorophenyl)ethyl]carbamate | HCID 57750386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 2-acetamido-1-(4-chlorophenyl)ethylcarbamate | HCID 57750416 | 62.7% |
Reaction Steps
A solution of tert-butyl 2-amino-1-(4-chlorophenyl)ethylcarbamate (Intermediate 73) (0.208 g, 0.77 mmol) and N-ethyldiisopropylamine (0.266 mL, 1.54 mmol) in THF (5 mL) was treated with acetic anhydride (0.102 mL, 1.08 mmol). The resulting solution was stirred at ambient temperature for 2 hours. The mixture was partitioned between DCM and sodium bicarbonate solution. The organic layer was concentrated and the residue was purified by flash column chromatography on silica using gradient elution (10% ethyl acetate/DCM to 40% ethyl acetate/DCM). The desired product, tert-butyl 2-acetamido-1-(4-chlorophenyl)ethylcarbamate (0.151 g, 62.7%), was thus isolated as a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101623B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-68bdbc6c635d484f94df78bc9ed2ddb4 |
| Source note | uspto-grants-2012_01 |