HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroquinone → N-(3-Morpholinopropyl)acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(3-Aminopropyl)morpholine | HCID 61055 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(3-Morpholinopropyl)acrylamide | HCID 11735756 | — |
Reaction Steps
In a 1 liter capacity round bottom flask equipped with a stirrer were put 90.5 g (1.0 mole) of acrylic acid chloride and 300 cc of acetonitrile and, as a polymerization inhibitor, 0.5 g of hydroquinone, and then, after the contents were cooled to 5°-10°C, 143 g (1.0 mole) of 3-morpholinopropylamine was added dropwise thereto over the course of 3.5 hours while stirring. Afterwards, the reaction mixture was stirred additionally for 2 hours at 40°-50°C. Next, a solution of 40 g of sodium hydroxide in 100 cc of water was added thereto and then the mixture was stirred for 30 minutes. After removal of the sodium chloride which separated, 152 g (77.0%) of a fraction of 144°-146°C/0.1 mmHg were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03957492 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-7faeb58b06b84401a87e5fa7555f3de7 |
| Source note | uspto-grants-1976_05 |