Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-(benzyloxy)acetate | HCID 290299 | — |
| Reactant | HCID 69027596 | HCID 69027596 | — |
| Product | HCID 57565029 | HCID 57565029 | 9.4% |
Reaction Steps
Reaction of the adduct of diethyl oxalate (14.61 g, 0.10 mol), ethyl benzyloxyacetate (19.42 g, 0.10 mol) and sodium hydride (4.40 g of a 60% dispersion in mineral oil, 0.11 mol) with 1-(2-hydroxyethyl)-4,5-dihydro-1H-imidazol-2-amine hydrobromide (21.0 g, 0.10 mol) as described for intermediate 1 gave 3.37 g (9% yield) of the title ester as white crystals; mp 104-106° C. (ethyl acetate-hexane). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.32 (3H, t, J=7.1 Hz, CH3), 3.53 (2H, m, CH2), 3.83 (2H, t, J=8.9 Hz, CH2), 3.90 (2H, m, CH2), 4.19 (2H, t, J=8.9 Hz, CH2), 4.32 (2H, q, J=7.1 Hz, OCH2), 5.11 (2H, s, OCH2), 7.35-7.40 (3H, m, aromatics), 7.51 (2H, m, aromatics). Anal. Calcd for C18H21N3O5: C, 60.16; H, 5.89, N 11.69. Found: C, 60.24; H, 5.89; N, 11.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494984B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-21bb7846f3294260a3cc53f78ef14d73 |
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| Source note | uspto-grants-2009_02 |
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