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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109054Generated: October 27, 2026

Sodium Bicarbonate → HCID 178501220, compound

https://huagongshe.com/reaction/2109054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl N-(2-oxoethyl)carbamateHCID 4247255—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178501210HCID 178501210—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 178501220HCID 17850122042%

Reaction Steps

Methyl trans-4-aminocyclohexanecarboxylate hydrochloride (1.22 g) obtained in Reference Example 2(1) is suspended in dichloromethane (10 ml), and thereto is added triethylamine (1.76 ml) and the mixture is stirred for several minutes. After a solution of t-butyl (2-oxoethyl)carbamate (1.00 g) in dichloromethane (5 ml) and sodium triacetoxy borohydride (1.46 g) are added successively under ice-cooling, the reaction solution is warmed to the room temperature and stirred for 15 hours. Saturated aqueous sodium hydrogen carbonate solution is poured to the reaction solution, and the mixture is extracted with chloroform. The organic layer is dried over sodium sulfate and evaporated to remove the solvent under reduced pressure. A portion (1.71 g) of the resulting residue (2.33 g) is purified by silica gel column chromatography (eluent: chloroform/methanol=10/1) to give methyl trans-4-({2-[(t-butoxycarbonyl)amino]ethyl}amino)cyclohexanecarboxylate (793 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514449B2
Source datasetuspto-grants-2009_04
ORD IDord-12db0ceeac764c3b93be6f98ec0df46d
Source noteuspto-grants-2009_04