HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Boc-L-Lys(Z)-OMe
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Boc-Lys(Z)-OH | HCID 2724765 | — |
| Solvent | Chloroform ethylacetate | HCID 21584013 | — |
| Product | Boc-L-Lys(Z)-OMe | HCID 11132998 | — |
Reaction Steps
An ethyl ether solution of 1.48 g (3.9 mmol) of Nε -benzyloxycarbonyl-Nα -(tert-butoxycarbonyl)-L-lysine was combined with an ethyl ether solution of diazomethane at 0° C. The reaction mixture was evaporated to give a colorless oil in nearly quantitative yield (1.54 g). TLC Rf =0.38 (chloroform/ethyl acetate, 5:1). IR (neat) ν 3340, 1710, 1530 cm-1. NMR (CDCl3) δ 7.3 (5H, s), 7.25 (1H, m), 5.05 (2H, s), 5.0 (1H, m), 4.1 (1H, m), 3.8 (3H, s), 3.1 (2H, m), 2.0-1.1 (6H, m), 1.4 (9H, s). The product has the structural formula: ##STR82##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05079366 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-97dc652a6fd84597abd1db3e6d8db2a6 |
| Source note | uspto-grants-1992_01 |