Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 54387449 | HCID 54387449 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19820418 | HCID 19820418 | 84% |
Reaction Steps
27.2 g of methyl 2-[4-chloro-2-[[(methylamino) carbonyl]methoxy]phenoxy]benzeneacetate was dissolved in 800 ml of dry tetrahydrofuran and slowly added to a suspension of 8.7 g lithium aluminum hydride in 800 ml of dry tetrahydrofuran. The reaction mixture was stirred overnight at 40° C. and after addition of 35 ml of water stirred for another 1 h. The salts were removed by filtration with suction and the filtrate was evaporated in vacuo, to give 20.1 g (84%) of 2-[4-chloro-2-[2- (methylamino)ethoxy]phenoxy]benzene ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05106839 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-1d8d96bf2a3145d2b5ca7ca2ef13b9bc |
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| Source note | uspto-grants-1992_04 |
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