HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl 2-((tert-butoxycarbonyl)amino)malonate → Diethyl 2-(2-benzyloxy-5-iodobenzyl)-2-tert-butoxycarbonylaminomalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl 2-((tert-butoxycarbonyl)amino)malonate | HCID 382219 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 1-Benzyloxy-2-bromomethyl-4-iodobenzene | HCID 11418231 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl 2-(2-benzyloxy-5-iodobenzyl)-2-tert-butoxycarbonylaminomalonate | HCID 66879924 | — |
Reaction Steps
41 g (101.7 mmol) of 1-benzyloxy-2-bromomethyl-4-iodobenzene (Example 4A) are added to a solution of 28 g (101.7 mmol) of diethyl 2-[N-(tert-butoxycarbonyl)amino]malonate and 7.9 ml (101.7 mmol) of sodium ethoxide in 300 ml of ethanol. After stirring at RT for 3 h, the precipitated product is collected by suction filtration. After drying in vacuo, 55 g (90% of theory) of product are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446102B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-8c030366cae84f828a34666b360855c4 |
| Source note | uspto-grants-2008_11 |