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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593469Generated: October 30, 2026

Triethylamine → (3R,4R)-1-tert-butyl 3-ethyl 4-(benzyloxycarbonyl)piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/1593469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(3R,4R)-1-tert-butyl 3-ethyl 4-aminopiperidine-1,3-dicarboxylateHCID 58745614—
SolventDichloromethaneHCID 6344—
Product(3R,4R)-1-tert-butyl 3-ethyl 4-(benzyloxycarbonyl)piperidine-1,3-dicarboxylateHCID 66952821188.1%

Reaction Steps

A solution of 252E (180 mg, 0.66 mmol) in CH2Cl2 (5 mL) was treated with benzyloxychloroformate (0.1 mL, 0.73 mmol) and triethylamine (0.12 mL, 0.86 mmol). The reaction was stirred at room temperature for 18 hours, diluted with CH2Cl2 (10 mL) and washed with water (2×10 mL), 0.1 N HCl (2×10 mL), saturated aqueous NaHCO3 (2×10 mL) and brine (1×10 mL). The organic layer was dried (Na2SO4), filtered and concentrated to give 243 mg (yield: 91%) of Compound 254A as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297695B2
Source datasetuspto-grants-2007_11
ORD IDord-258b27f6f359447cb3a00382f0a4d7bf
Source noteuspto-grants-2007_11