HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 54053136, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 54405952 | HCID 54405952 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54053136 | HCID 54053136 | — |
Reaction Steps
Potassium t-butoxide (810 mg) was added to a solution of [1-(2-hydroxyethyl)-1,2,3,4-tetrahydronaphthalen-5-yloxy]acetic acid ethyl ester (2.11 g, prepared by the same procedure as in reference example 1) in dimethylformamide (50 ml) at 0° C. The reaction mixture was stirred for 1 hr at room temperature. Benzhydryl bromide (2.15 g) was added to the mixture at 0° C. The mixture was stirred for 1 hr at room temperature. To the mixture, a saturated aqueous solution of ammonium chloride and ether were added. The extract was washed with water and saturated brine, dried over magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (n-hexane: ethyl acetate=8: 2) to give the title compound (257 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05461045 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-ccb5ff88518547f08a9e6df1bdc9193d |
| Source note | uspto-grants-1995_10 |