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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444713Generated: October 28, 2026

Water → 4-(Benzyl-tert-butoxycarbonylmethyl-amino)-cyclohexanecarboxylic acid tert-butyl ester

https://huagongshe.com/reaction/444713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl bromoacetateHCID 79177—
Reactant4-Benzylamino-cyclohexanecarboxylic acid tert-butyl esterHCID 68724841—
SolventDimethylformamideHCID 6228—
Product4-(Benzyl-tert-butoxycarbonylmethyl-amino)-cyclohexanecarboxylic acid tert-butyl esterHCID 6872548634.1%

Reaction Steps

To a solution of 4-benzylamino-cyclohexanecarboxylic acid tert-butyl ester (630 mg, 2.180 mmol) in DMF (20 mL) is added t-butyl bromoacetate (1 mL, 6.856 mmol) and Cs2CO3 (1.0 g, 3.069 mmol). The mixture stirs for 2 h. Then H2O (50 mL) is added the mixture is extracted with EtOAc (2×100 mL), dried with sodium sulfate and concentrated. The resulting solid is purified by flash chromatography (gradient elution: 0-20% EtOAc/Hep) which affords 300 mg of 4-(benzyl-tert-butoxycarbonylmethyl-amino)-cyclohexanecarboxylic acid tert-butyl ester. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.24 (m, 5 H), 1.38 (m, 18 H), 1.86 (m, 4 H), 2.09 (m, 1 H), 3.14 (m, 2 H), 3.71 (m, 2 H), 7.29 (m, 5 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476224B2
Source datasetuspto-grants-2013_07
ORD IDord-72b62785338849809cd646c9d5eeec49
Source noteuspto-grants-2013_07