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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868572Generated: November 4, 2026

Hydrochloric Acid → HCID 69029202, compound

https://huagongshe.com/reaction/1868572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2',4'-DihydroxyacetophenoneHCID 6990—
ReactantEthyl 3,5-bis(benzyloxy)benzoateHCID 3016563—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69029202HCID 69029202—

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 20% lithiumhexamethyldisilazane in tetrahydrofuran (217.5 mL, 260 mmol) was added to a well-stirred solution of 2,4-dihydroxy acetophenone, 14 (9.88 g, 65 mmol) in tetrahydrofuran (150 mL) under nitrogen atmosphere at −78° C. for 30 min. The reaction mixture was stirred at −78° C. for 1 h and at −30° C. for 2 h. It was again cooled to −78° C. and a solution of ethyl-3,5-dibenzyloxy-benzoate 8 (23.5 g, 65 mmol) in tetrahydrofuran (100 mL) was added over a period of 30 min. It was further stirred at room temperature for overnight and poured into ice water containing hydrochloric acid. It was extracted with chloroform, dried over sodium sulphate, filtered and evaporated on rotavapor to afford 1-(3,5-bis-benzyloxy-phenyl)-3-(2,4-dihydroxy-phenyl)-propane-1,3-dione (16). The residue, 16 (37.8 g) was refluxed with Dowex-H+ (8 g) in 2-propanol (300 mL) for 34 h. 2-Propanol was evaporated on rotavapor, residue suspended in hot dimethyl formamide and filtered. The filtrate was 3,4-Dimethoxy-benzoic acid (10). Yield 2 g (8%); mp 179-181° C.; MS (FAB) 183 (M++1); IR (KBr) 2939, 2836, 1867, 1678; 1H NMR (200 MHz, CDCl3) δ 7.79 (dd, J=8.4 Hz, 1.9 Hz, 1H), 7.60 (d, J=1.8 Hz, 1H), 6.93 (d, J=8.5 Hz, 1H), 3.96 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635779B2
Source datasetuspto-grants-2009_12
ORD IDord-1fe4fdc7c90c406d9fcff0e89dbbb623
Source noteuspto-grants-2009_12