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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650180Generated: October 30, 2026

6-Bromo-2-naphthalenol → HCID 21883581, compound

https://huagongshe.com/reaction/650180

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2-naphthalenolHCID 27144—
Reactantethyl 6-chloro-7-fluoro-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 21883602—
SolventWaterHCID 962—
ProductHCID 21883581HCID 21883581—

Reaction Steps

The title compound was prepared from 6-bromo-2-napthol 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 252.6-254.8° C. 1H NMR (acetone-d6/300 MHz) 8.19 (s, 1H), 8.04 (d, 1H, J=9.1 Hz), 7.93 (s, 1H), 7.87 (d, 1H, J=8.9 Hz), 7.75 (s, 1H), 7.65 (d, 1H, J=8.8 Hz), 7.55 (s, 1H), 7.43 (d, 1H, J=9.1 Hz), 6.72 (s, 1H), 5.83 (q, 1H, J=7.0 Hz). 19F NMR (acetone-d6/282 MHz) −79.4 (d, J=6.5 Hz). FABLRMS m/z 497 (M−H). ESHRMS m/z 496.9421 (M−H, Calc'd 496.9403). Anal. Calc'd for C21H11BrClF3O4 with 1.75 wt % H2O: C, 49.60; H, 2.38; Br, 15.71; Cl, 6.97. Found: C, 49.55; H, 2.03; Br, 15.56; Cl, 7.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271253B1
Source datasetuspto-grants-2001_08
ORD IDord-58098bb69ede43dcac4cd2b7d59eecca
Source noteuspto-grants-2001_08