HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Glycolate → Ethyl 2-((4-nitrophenoxy)carbonyloxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Glycolate | HCID 12184 | — |
| Reactant | 3-Bromobenzyl alcohol | HCID 85141 | — |
| Reactant | 3-Bromobenzyl 4-nitrophenyl carbonate | HCID 86712580 | — |
| Product | Ethyl 2-((4-nitrophenoxy)carbonyloxy)acetate | HCID 69126482 | — |
Reaction Steps
The title compound was prepared using a procedure analogous to 3-bromobenzyl 4-nitrophenyl carbonate except that (3-bromophenyl)methanol was replaced with ethyl 2-hydroxyacetate. LCMS, [M+Na]+=292.0. 1H NMR (400 MHz, CDCl3) δ 8.24 (d, J=9.2 Hz, 2H), 7.37 (d, J=9.2 Hz, 2H), 4.72 (s, 2H), 4.25 (q, J=7.2 Hz, 2H), 1.28 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062028B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-07c9f0c70cd44b0c84d4665c98dc0f3f |
| Source note | uspto-grants-2015_06 |