HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626388Generated: October 30, 2026
Potassium Carbonate → tert-Butyl 7-(4-carbamoylphenoxy)-6-cyanochroman-4-carboxylate
https://huagongshe.com/reaction/1626388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxybenzamide | HCID 65052 | — |
| Reactant | Tert-butyl 6-cyano-7-fluorochroman-4-carboxylate | HCID 67288243 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | tert-Butyl 7-(4-carbamoylphenoxy)-6-cyanochroman-4-carboxylate | HCID 86664391 | 83.2% |
Reaction Steps
tert-butyl 6-cyano-7-fluorochroman-4-carboxylate (290 mg, 1.05 mmol), 4-hydroxybenzamide (172 mg, 1.25 mmol) and potassium carbonate (347 mg, 2.51 mmol) were diluted with dry NMP (4 mL). The reaction was bubbled with argon for 10 minutes and then heated at 120° C. for 12 hours under a slight argon bubble. The reaction was cooled and loaded directly onto a biotage 40 M cartridge, eluting with 20% ethyl acetate/hexanes to 100% ethyl acetate to yield 1 g of the crude product which was found to contain NMP. The residue was taken up in ethyl acetate and washed twice with water and then brine. The organic layer was dried over magnesium sulfate, filtered and concentrated to provide the desired product (343 mg, 83.2% yield) as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785445B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-7e69ab0e696b4935b8d04bf867f93f50 |
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| Source note | uspto-grants-2014_07 |
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