HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 66625110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl (4-aminophenyl)carbamate | HCID 688611 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66625110 | HCID 66625110 | 94% |
Reaction Steps
Step A To a solution of N-Boc-1,4-phenylene diamine (Aldrich, 1.00 g, 4.82 mmol) in CH2Cl2 (12 ml) were added N,N-diisopropylethylamine (1.26 g, 9.76 mmol) and ethyl bromoacetate (Aldrich, 813 mg, 4.87 mmol). The mixture was allowed to stir at rt overnight and then taken up in EtOAc (300 ml) and washed with sat. aqueous Na2CO3, water and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to give ethyl 2-(4-(tert-butoxycarbonylamino)phenylamino)acetate as a light brown oil (1.33 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088815B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2bc3a7a169a64e9a85d92dcb2646ffeb |
| Source note | uspto-grants-2012_01 |