HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl methyl ether → 1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl methyl ether | HCID 83093 | — |
| Reactant | 1-Bromo-4-chloro-2-fluorobenzene | HCID 137275 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzene | HCID 68809381 | 71% |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in THF (50 mL) was slowly added to LDA (0.125 mol) in THF (600 mL) at −50° C. After addition the solution was warmed to −20° C. and then cooled to −50° C. a solution of bromomethoxymethane (25 g, 0.200 mol) in THF (25 mL) was slowly added and the reaction mixture was warmed to ambient temperature. The reaction was quenched with water (400 mL) and extracted with diethyl ether (2×150 mL). The combined organic phases were dried (sodium sulfate) and concentrated. The residual oil was distilled (70°-75° C./0.5 mm) to give 1-bromo-4-chloro-2-fluoro-3-methoxymethylbenzene (18.0 g, 0.071 mol): 1H NMR (CDCl3): δ 7.50 (m, 1H), 7.15 (dd, 1H), 4.65 (s, 1H), 3.40 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07314849B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-ac2da014daba480d85a8943209a2482b |
| Source note | uspto-grants-2008_01 |