HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 66679455, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 66680028 | HCID 66680028 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66679455 | HCID 66679455 | — |
Reaction Steps
To a solution of 6.35 g (15.4 mmol) of (3-aminopropyl)-(4-benzyloxycarbonyl-aminobutyl)-carbamic acid benzyl ester (Synth. Commun. 2005, 35, 1085) in 200 mL of acetonitrile, and 2.6 mL (1.86 g, 15.4 mmol) of triethylamine, there are introduced, with stirring, at ambient temperature, 1.70 mL (2.56 g, 15.4 mmol) of ethyl bromoacetate. Stirring is maintained for 4 hours. The reaction mixture is poured into water and extracted with ethyl acetate. The organic phases are separated off and then dried over sodium sulfate, filtered and evaporated. 7.7 g of an oil are obtained, which is used directly in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08664409B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-468f6992bafc49b082090652232da049 |
| Source note | uspto-grants-2014_03 |