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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051209Generated: November 1, 2026

Acetic Acid → HCID 90102892, compound

https://huagongshe.com/reaction/1051209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantTert-butyl 3-nitrophenylcarbamateHCID 10514065—
ReactantHCID 178418680HCID 178418680—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90102892HCID 9010289273.4%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of (3-nitro-phenyl)-carbamic acid tert-butyl ester (1.20 g, 5.04 mmol) in THF (50 mL) was added ((trimethylsilyl)methyl)magnesium chloride (1.48 g, 10.1 mmol) at −70° C. under nitrogen gas. The solution was then stirred at −70° C. for one h. A solution of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (2.74 g, 12.1 mmol) in THF (30 mL) was added, the reaction was warmed to 0° C. and the reaction was allowed to stir at 0° C. for another hour. The reaction mixture is poured into an aqueous solution of acetic acid (50 mL, 5%v/v) and the aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried over magnesium sulfate. Filtration followed by concentration in vacuo gave a brown oil. Flash chromatography (80/20 hexanes/ethyl acetate) afforded (3-nitro-4-trimethylsilanylmethyl-phenyl)-carbamic acid tert-butyl ester (1.20 g, 73%) as a light oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388166B2
Source datasetuspto-grants-2016_07
ORD IDord-64dfc5c41f0b4b819fad899a811ec854
Source noteuspto-grants-2016_07