Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-{4-[2-(Allyloxy)-ethyl]phenoxy}-3-isopropylamino propan-2-ol | HCID 11659338 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Betaxolol | HCID 2369 | — |
Reaction Steps
To a stirred solution of compound of formula (1) (1 g, 0.003 mol) in dry toluene (5 ml), diethylzinc (1.1 M solution in toluene, 14 ml, 0.017 mol) was added at 0° C. under nitrogen atmosphere followed by diiodomethane (1.38 ml, 0.017 mol). The reaction was stirred for 16 h at 0° C. and poured over cold aqueous solution of ammonium chloride. The organic layer was separated and the aqueous layer extracted repeatedly with toluene. The combined organic layer was washed with a solution of sodium thiosulphate, dried over anhydrous sodium sulphate, filtered and concentrated to yield racemic betaxolol of formula (2) 1.6 g (84%) mp 70 –72° C. as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07227039B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-d4a41da84d1d4cb7a3440d8420287f4f |
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| Source note | uspto-grants-2007_06 |
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