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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421617Generated: November 2, 2026

3-Hydroxybenzoic Acid → HCID 21883503, compound

https://huagongshe.com/reaction/1421617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxybenzoic AcidHCID 7420—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 6-chloro-7-fluoro-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 21883602—
ProductHCID 21883503HCID 21883503—

Reaction Steps

The title compound was prepared from 3-hydroxybenzoic acid and ethyl 6-chloro-7-fluoro-2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylate (Example 183, Step 2) via a procedure similar to that described in Example 183, Steps 3 and 4. (Note: In the step similar to step 3, an additional equivalent of potassium carbonate was added.) mp 288.1-289.2° C. 1H NMR (acetone-d6 /300 MHz) 7.92 (m, 2H), 7.75 (s, 1H), 7.68 (d, 1H, J=1.4 Hz), 7.62 (t, 1H, J=7.9 Hz), 7.41 (m, 1H), 6.72 (s, 1H), 5.85 (q, 1H, J=7.0 Hz). 19F NMR (acetone-d6 /282 MHz) -79.4 (d, J=6.5 Hz). ESHRMS m/z 413.0027 (M-H, Calc'd 113.0040). Anal. Calc'd for C18H10ClF3O6 : C, 52.13; H, 2.43; Cl, 8.55. Found: C, 51.88; H, 2.48; Cl, 8.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077850
Source datasetuspto-grants-2000_06
ORD IDord-8b8562a4b5a044d88ec692252cfebf45
Source noteuspto-grants-2000_06