HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 10987985, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Ketone, 2,4-dimethylpyrrol-3-yl methyl | HCID 15163 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 10987985 | HCID 10987985 | — |
Reaction Steps
A solution of 10 ml of aqueous hydriodic acid, 10 ml of acetic anhydride and 2 ml of 50% hypophosphorous acid containing 548 mg of 2,4-dimethyl-3acetyl pyrrole was stirred magnetically while a solution of 0.6 ml of benzaldehyde in 5 ml of acetic anhydride was slowly added over 20 mins. The solution was stirred for 10 mins, then poured into water. The crude product which separated was recrystallized from acetone (thimble) as nearly colourless irregular plates (85%, m.p. 165.5°-167° C. after a partial change to prismatic rods above 165° C. Anal. Cal. for C15H17NO: C, 79.26; H, 7.54; N, 6.16. Found: C, 79.22; H, 7.50; N, 6.18.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04070366 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-07403b26b50e48a1aa0376b113c057e5 |
| Source note | uspto-grants-1978_01 |