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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722296Generated: October 30, 2026

Hydrochloric Acid → HCID 21883633, compound

https://huagongshe.com/reaction/722296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 53638824HCID 53638824—
ReactantHCID 69662645HCID 69662645—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21883633HCID 2188363395%

Reaction Steps

Preparation of 2-trifluoromethyl-3H-naphthopyran-carboxylic acid. A solution of the ester from Step 1 (0.8 g, 2.5 mmol) was dissolved in 40 mL of ethanol and 10 mL of tetrahydrofuran, treated with sodium hydroxide (2.5 N, 10 mL, 25 mmol) and stirred at room temperature for 16 hours. The reaction mixture was acidified with 1.0 N HCl, whereupon a solid formed that was isolated by filtration. The solid was washed with 20 mL of water to afford 0.7 g (95%) of the title compound as a yellow solid: mp 245.9–248.6° C. 1H NMR (acetone-d6/300 MHz) 8.57 (s, 1H), 8.28 (d, 1H, J=8.7 Hz), 8.03 (d, 1H, J=9.0 Hz), 7.93 (d, 1H, J=8.7), 7.67 (m, 1H), 7.50 (m, 1H), 7.28 (d, 1H, J=9.0), 5.96 (qH-F, 1H, J=7.2 Hz). FABHRMS m/z 295.0561 (M+H, Calc'd 295.0582). Anal. Calc'd for C15H9O3F3+3.31% H2O: C, 59.21; H, 3.35. Found: C, 59.17; H, 3.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138411B2
Source datasetuspto-grants-2006_11
ORD IDord-617dab899ffd4615b502ab9fe49fd7b1
Source noteuspto-grants-2006_11