HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867986Generated: October 31, 2026
Dimethylformamide → HCID 67873983, compound
https://huagongshe.com/reaction/867986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-{2-[2-(2-Chloroethoxy)ethoxy]ethoxy}oxane | HCID 13416507 | — |
| Reactant | HCID 15117887 | HCID 15117887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67873983 | HCID 67873983 | 64.5% |
Reaction Steps
A mixture of methyl 5-t-octylsalicylate (37.7 g, 0.143 mole), 2-(2-[2-(2-chloroethoxy)ethoxy]ethoxy)tetrahydropyran (54 g, 0.214 mole), potassium carbonate (28 g, 0.217 mole) and N,N-dimethylformamide (250 ml) was heated at 140° C., under nitrogen, for 18 hours, with stirring. The mixture was cooled, diluted with ether, and then washed liberally with saturated sodium chloride solution. The ethereal solution was dried (MgSO4) and evaporated in vacuo to give an oil, which was chromatographed on silica gel to give 46 g of methyl 2-(2-[2-(2-[2-tetrahydropyranyloxy]ethoxy)ethoxy]ethoxy)-5-t-octylsalicylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04777270 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-a997f710c0e44781a87f096ea4431db6 |
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| Source note | uspto-grants-1988_10 |
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