Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100160Generated: November 2, 2026

Hydrochloric Acid → HCID 57757225, compound

https://huagongshe.com/reaction/2100160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86613511HCID 86613511—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57757225HCID 5775722597.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

Ethyl({4-[cycloheptylidene(4-hydroxyphenyl)methyl]phenyl}oxy)acetate (190) (0.20 g, 0.53 mmol) was dissolved in THF and EtOH (1:1, 6 mL). To the above solution was added 1 N NaOH (2.5 mL) at room temperature. The reaction was heated at 70° C. with stirring for 0.5 h and then cooled at RT. Reaction mixture was acidified with 20% aqueous HCl, and then extracted with EtOAc. The organic layer washed with brine, dried (Na2SO4), and concentrated under reduced pressure to afford the crude product. The product was purified by flash column chromatography with chloroform and methanol (9:1 to 4:1) as an eluent to give 0.182 g of compound 191 as an off-white solid. mp 170-171° C. 1H NMR (300 MHz, DMSO-d6): δ 12.92 (s, 1H), 9.25 (s, 1H), d, J=8.4 Hz, 2H), 6.89 (d, J=8.4 Hz, 2H), 6.81 (d, J=8.7 Hz, 2H), 6.66 (d, J=8.4 Hz, 2H), 4.62 (s, 2H), 2.22 (br s, 4H), 1.5 (br s, 8H). LCMS (ESI): m/z 375.08 (M+Na)+. Anal. Calcd for C22H24O4: C, 74.98; H, 6.86; Found: C, 73.05; H, 6.74.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569601B2
Source datasetuspto-grants-2009_08
ORD IDord-08b78c0a8031483cae45aa788a23437c
Source noteuspto-grants-2009_08