HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl iodoacetate → [2-(2-Chloro-6-fluoro-phenyl)-ethoxy]-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl iodoacetate | HCID 12183 | — |
| Reactant | 2,6-Di-tert-butylpyridine | HCID 68510 | — |
| Reactant | 2-(2-Chloro-6-fluorophenyl)ethanol | HCID 2733235 | — |
| Catalyst | Silver(I) trifluoromethanesulfonate | HCID 76223 | — |
| Product | [2-(2-Chloro-6-fluoro-phenyl)-ethoxy]-acetic acid ethyl ester | HCID 68564810 | — |
Reaction Steps
In analogy to the procedure described in example 78.1, 2-(2-chloro-6-fluoro-phenyl)-ethanol was reacted with ethyl iodoacetate in the presence of silver trifluoromethanesulfonate and 2,6-di-tert-butylpyridin to give [2-(2-chloro-6-fluoro-phenyl)-ethoxy]-acetic acid ethyl ester as colorless liquid. 1H NMR (CDCl3): 1.28 (t, J=7.1 Hz, 3H), 3.15 (t, J=7.1 Hz, 2H), 3.73 (t, J=7.3 Hz, 2H), 4.11 (s, 2H), 4.22 (q, J=7.1 Hz, 2H), 6.96 (m, 1H), 7.09-7.19 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07572801B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-52554209fc5a4679b5c26c45f7c589c9 |
| Source note | uspto-grants-2009_08 |