HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733286Generated: November 1, 2026
N,N,N',N'-Tetramethylmethanediamine → HCID 20301086, compound
https://huagongshe.com/reaction/1733286
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylmethanediamine | HCID 5829 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 10084425 | HCID 10084425 | — |
| Product | HCID 20301086 | HCID 20301086 | — |
Reaction Steps
A mixture of 1.35 g (5 mmol) of 3'-nitroflavanone [prepared as described in J. Chem. Soc. Japan, Pure Chem. Sect. 74, 827 (1953)], and 12 ml of bis-(dimethylamino)methane was stirred at room temperature; 12 ml of acetic anhydride was added dropwise over 15 minutes. The temperature rose to 77°. After cooling to ambient temperature, the reaction was partitioned between 100 ml portions of ether and 100 ml portions of cold water. The aqueous phase was separated, washed with two 100 ml 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 100 g of silica gel, eluting with benzene to yield 548 mg of 3'-nitro-3-methylene flavanone, isolated as a white solid, m.p. 131°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04241069 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-c7d6b59242294f579facfdca4aeaf05e |
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| Source note | uspto-grants-1980_12 |
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