HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Boc-L-glutamine methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | L-Glutamine, N2-((1,1-dimethylethoxy)carbonyl)- | HCID 83687 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Boc-L-glutamine methyl ester | HCID 10956293 | 100% |
Reaction Steps
To a solution of BOC-L-Gln (20 g, 81 mmol) in 50 mL of EtOAC and MeOH at 0° C. was added diazomethane in 250 mL of Et2O with stirring. The resulting yellow solution was stirred at 0° C. for 5 minutes and then warmed up to room temperature and stirred for 20 minutes. Argon gas was then bubbled through the yellow reaction mixture to remove excess diazomethane. The crude product was concentrated and purified by crystallization from methyl-tert-butyl ether. Yield 100%. 1H NMR (CDCl3) δ 1.45 (s, 9H), 1.96 (m, 1H), 2.21 (m, 1H), 2.36 (m, 2H), 3.76 (s, 3H,), 4.34 (m, 1H), 5.32 (m, 1H), 5.44 (bs, 1H), 6.16 (bs, 1H). Anal. (C11H20N2O5) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214799B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-eca7167245714374b68549ed6db9afcc |
| Source note | uspto-grants-2001_04 |