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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421598Generated: November 3, 2026

p-(Trifluoromethoxy)phenol → 6-Chloro-2-(trifluoromethyl)-7-[4-(trifluoromethoxy)phenoxy]-2H-1-benzopyran-3-carboxylic acid

https://huagongshe.com/reaction/1421598

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(Trifluoromethoxy)phenolHCID 70015—
Reactantethyl 6-chloro-7-fluoro-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 21883602—
Product6-Chloro-2-(trifluoromethyl)-7-[4-(trifluoromethoxy)phenoxy]-2H-1-benzopyran-3-carboxylic acidHCID 15458906—

Reaction Steps

The title compound was prepared from 4-(trifluoromethoxy)phenol 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: mp 198.0-199.2° C. 1H NMR (acetone-d6 /300 MHz) 7.91 (s, 1H), 7.73 (s, 1H), 7.43 (d, 2H, J=9.1 Hz), 7.25 (d, 2H, J=9.1 Hz), 6.70 (s, 1H), 5.82 (q, 1H, J=7.0 Hz). 19F NMR (acetone-d6 /282 MHz) -59.4 (s, 3F), -79.4 (d, 3F, J=7.2 Hz). ESLRMS m/z 453 (M-H). ESHRMS m/z 452.9950 (M-H, Calc'd 452.9964). Anal. Calc'd for C18H9ClF6O5 : C, 47.55; H, 2.00; Cl, 7.80. Found: C, 47.47; H, 1.89; Cl, 8.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077850
Source datasetuspto-grants-2000_06
ORD IDord-282bb651905240ae88f5d44321924350
Source noteuspto-grants-2000_06