HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylamide → 2-(Cyclopropylmethoxy)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylamide | HCID 5147 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Cyclopropylmethoxy)benzamide | HCID 2728029 | — |
Reaction Steps
Salicylamide (15.22 g), potassium hydroxide (85%, 7.73 g) and cyclopropylmethyl bromide (16.024 g) were heated together under reflux in absolute ethanol (100 ml) for 91/2 hours. The cooled mixture was filtered to remove inorganic products and the filtrate was evaporated to an oil. The oil was dissolved in 1:1 toluene:ethyl acetate (200 ml) and the solution was washed with 10% potassium hydroxide solution (2×30 ml), water (50 ml) and saturated brine (50 ), dried (Na2SO4), and concentrated under reduced pressure, leaving 2-(cyclopropylmethoxy)benzamide as an oil which crystallised (17.606 g, 83%), mp 95°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106843 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-d486e383ce8148c69dfcb0b8c369f281 |
| Source note | uspto-grants-1992_04 |