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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188873Generated: November 2, 2026

Hydrochloric Acid → HCID 86652834, compound

https://huagongshe.com/reaction/1188873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 46941671HCID 46941671—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 86652834HCID 8665283491%

Reaction Conditions

Temperature-5 °C

Reaction Steps

2-(Benzyloxy)-4-[4-(methylsulfonyl)phenoxy]aniline (43.8 g) was suspended in a mixed solvent of acetonitrile (50 mL)-ethanol (400 mL), and concentrated hydrochloric acid (25 mL) was added at 10° C. Then, ethanol (100 ml) was added. Sodium nitrite (9.8 g) dissolved in water (16 mL) was added dropwise at −5 to 0° C., and the mixture was stirred at −5° C. for 30 min. Water (100 mL) was added to reaction mixture, and the mixture was added dropwise to a mixture of ethyl 2-methyl-3-oxobutanoate (18.8 mL), potassium hydroxide (85%, 23 g), water (100 mL) and ethanol (100 mL) over 2 hr at −13° C. to −11° C. The reaction mixture was stirred at −11° C. for 40 min, and the precipitated orange solid was collected by filtration. The obtained solid was washed with ethanol and diethyl ether to give the title compound (52.3 g, yield 91%) as orange crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673942B2
Source datasetuspto-grants-2014_03
ORD IDord-272353bfe01143ebb5da99a6d3f2733f
Source noteuspto-grants-2014_03