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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722367Generated: October 29, 2026

2-Bromo-4-chlorophenol → HCID 21883543, compound

https://huagongshe.com/reaction/722367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-chlorophenolHCID 69670—
Reactantethyl 6-chloro-7-fluoro-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 21883602—
ProductHCID 21883543HCID 21883543—

Reaction Steps

The title compound was prepared from 2-bromo-4-chlorophenol 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 223.6–225.6° C. 1H NMR (acetone-d6/300 MHz) 7.89 (s, 1H), 7.83 (d, 1H, J=2.6 Hz), 7.73 (s,1H), 7.52 (dd, 1H, J=8.7 Hz, 2.4 Hz), 7.25 (d, 1H, J=8.9 Hz), 6.55 (s, 1H), 5.83 (q, 1H, J=7.0 Hz). 19F NMR (acetone-d6/282 MHz) −79.4 (d, J=7.2 Hz). FABLRMS m/z 481 (M−H). ESHRMS m/z,480.8856 (M−H, Calc'd 480.8857). Anal. Calc'd for C17H8BrCl2F3O4: C, 42.18; H, 1.67; Br, 16.51; Cl, 14.65. Found: C, 42.15; H, 1.54; Br, 16.56; Cl, 14.39.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138411B2
Source datasetuspto-grants-2006_11
ORD IDord-391fff7e534f45ad83838c2b80480676
Source noteuspto-grants-2006_11