HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → 2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyl-3-(1-hydroxymethylethoxy)-4-nitrophenyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyl-3-(1-carbethoxyethoxy)-4-nitrophenyl ether | HCID 86735057 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Chloro-alpha,alpha,alpha-trifluoro-p-tolyl-3-(1-hydroxymethylethoxy)-4-nitrophenyl ether | HCID 86735748 | — |
Reaction Steps
A solution of 2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-carbethoxyethoxy)-4-nitrophenyl ether (17.32 g, 0.04 mole) in dry ether (500 ml) is treated at -10° C. with a suspension of lithium aluminum hydride (1.9 g) in ether (approximately 100 ml) added with stirring over ten seconds. The termperature increases to about 0° to 10° C. and after a total of 45 seconds, the reaction mixture is quenched by pouring, with stirring, onto ice/dilute sulfuric acid. The ether phase is washed with water, dried, filtered through activated silica gel, and the solvent removed to give 2-chloro-α,α,α-trifluoro-p-tolyl-3-(1-hydroxymethylethoxy)-4-nitrophenyl ether as a dark oil, yield 14 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04613360 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-1fab41bf21ef4605b1d4936cc2dd7a86 |
| Source note | uspto-grants-1986_09 |