HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N,N',N'-Tetramethylmethanediamine → 2',4'-Dichloro-3-methylene flavanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N,N',N'-Tetramethylmethanediamine | HCID 5829 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2',4'-Dichloro flavanone | HCID 12753173 | — |
| Product | 2',4'-Dichloro-3-methylene flavanone | HCID 12753176 | — |
Reaction Steps
A mixture of 3 g (10 mmol) of the 2',4'-dichloro flavanone and 27 ml of bis-(dimethylamino)methane was stirred at room temperature; 27 ml of acetic anhydride was added dropwise over 15 minutes. A slight temperature rise occurred. One hour later the reaction was partitioned between 200 ml of ether and 200 ml of cold H2O. The aqueous phase was separated, washed with two 250 ml portions of ether, and discarded. The combined ether extracts were washed with saturated aqueous NaHCO3 solution, dried over anhydrous Na2SO4, filtered and evaporated. The residual oil was chromatographed on 200 g of silica gel, eluting with benzene. This gave 2.5 g of 2',4'-dichloro-3-methylene flavanone, isolated as a solid, m.p. 86°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04241069 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-47bfabade6934224bfb8b57d44e9e5cf |
| Source note | uspto-grants-1980_12 |