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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892486Generated: October 28, 2026

Water → Tert-butyl 2-(4-hydroxyphenyl)ethyl hydrazine-1,2-dicarboxylate

https://huagongshe.com/reaction/1892486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTyrosolHCID 10393—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactanttert-Butyl carbazateHCID 70091—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(4-hydroxyphenyl)ethyl hydrazine-1,2-dicarboxylateHCID 5811215320.8%

Reaction Steps

To a suspension of 1,1′-carbonyldiimidazole (1.620 g, 9.989 mmol) in anhydrous tetrahydrofuran (20 ml) was added 2-(4-hydroxyphenyl)ethanol (1.383 g, 10.01 mmol), and the mixture was stirred at room temperature for 3 hr. tert-Butyl carbazate (1.323 g, 10.01 mmol) was added, and the mixture was stirred at room temperature for 1.5 hr. Water (100 ml) and ethyl acetate (100 ml) were added to the reaction mixture, and the mixture was stirred, stood still and then partitioned. The aqueous layer was extracted with ethyl acetate, and the combined organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (FUJI SILYSIA CHEMICAL LTD. BW-300SP 40 g, ethyl acetate:hexane=4:6→5:5). The fractions containing the object product were concentrated under reduced pressure, and the obtained solid was suspended in diisopropyl ether (50 ml) and filtered. The filtered product was washed 3 times with diisopropyl ether and dried under reduced pressure to give tert-butyl 2-(4-hydroxyphenyl)ethyl hydrazine-1,2-dicarboxylate (616.7 mg, 2.08 mmol, yield 20.8%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507690B2
Source datasetuspto-grants-2013_08
ORD IDord-d1303a1642f8424bba48a15f0d0044d6
Source noteuspto-grants-2013_08