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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868251Generated: November 3, 2026

Water → HCID 66643089, compound

https://huagongshe.com/reaction/1868251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
ReactantDi-tert-butyl IminodicarboxylateHCID 279800—
ReactantMethyl 2-(bromomethyl)-6-nitrobenzoateHCID 21708527—
CatalystLithium iodideHCID 66321—
SolventMethyl Ethyl KetoneHCID 6569—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 66643089HCID 6664308994%

Reaction Conditions

Temperature100 °C

Reaction Steps

A stirred mixture of 2-bromomethyl-6-nitro-benzoic acid methyl ester (36.6 g, 134 mmol), di-tert-butyl iminodicarboxylate (29.1 g, 134 mmol), cesium carbonate (89.3 g, 274 mmol), and lithium iodide (0.89 g, 6.7 mmol) in 2-butanone (400 mL) was heated to reflux in a 100° C. oil bath for 12 hours while stirred with a mechanical stirrer. The mixture was allowed to cool to room temperature. To the mixture, was add brine (300 mL), water (300 mL), ethyl acetate (750 mL) and stirred for 10 minutes, then the suspension was filtered through a pad of Celite. The two layers were separated, and the organic layer was evaporated to a less volume and the aqueous layer was extracted with ethyl acetate (2×150 mL). The combined organic layers were washed with brine (500 mL), dried over magnesium sulfate while de-colored at the same time with charcoal at room temp for 30 minutes. The black mixture was filtered through a pad of Celite. The filtrate was evaporated to give 2-(di-tert-butoxycarbonylamino-methyl)-6-nitro-benzoic acid methyl ester as a brown oil (51.53 g, 94% yield). The product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635700B2
Source datasetuspto-grants-2009_12
ORD IDord-62532d59f727480abb386824625c5c02
Source noteuspto-grants-2009_12