HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248554Generated: October 28, 2026
Dimethylformamide → HCID 20095713, compound
https://huagongshe.com/reaction/248554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 20095706 | HCID 20095706 | — |
| Product | HCID 20095713 | HCID 20095713 | — |
Reaction Steps
43.6 g of 5-bromo-2,4-diethoxy-6-methyl-1-methoxymethyloxybenzene prepared in Referential Example 8 was dissolved in 220 ml of THF, and 100 ml of n-buthyllithium (1.6 M n-hexane solution) was dropwise added thereto at -70° C. The mixture was stirred at -40° C. for 30 min, and 11.9 g of dimethylformamide was dropwise added thereto. The temperature of the reaction mixture was returned to room temperature, and an aqueous ammonium chloride solution was added thereto,-followed by extracting with ethyl acetate. The organic phase was washed with water, dried, concentrated and purified by silica gel column chromatography (eluent; n-hexane : ethyl acetate=90 : 10) to prepare 19.2 g of the product compound as a colorless oleaginous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05210239 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-9085fcc9bd1e485fb332a0dc44c9ceac |
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| Source note | uspto-grants-1993_05 |
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