HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 1-(Allyloxy)-3-aminopropan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Allyl glycidyl ether | HCID 7838 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Product | 1-(Allyloxy)-3-aminopropan-2-ol | HCID 98015 | — |
Reaction Steps
Ammonium hydroxide (28%–30% (about 14.82 mol) of ammonia in water, 202 mL, 3 mol) was charged to a one liter, one-neck, round-bottom flask that was cooled in an ice bath. To the above solution allyl glycidyl ether (57.07 g, 0.5 mol) was added dropwise at 0° C. The mixture was allowed to warm up to room temperature and stirred for two days after completion of the allyl glycidyl ether addition. 3-Allyloxy-2-hydroxy-propylamine was separated by distillation at 76° C.–82° C. under 0–1 mbar as a clear liquid (˜33 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214809B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-bc64c61b49ce4690a4aefedd09313088 |
| Source note | uspto-grants-2007_05 |