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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905950Generated: October 28, 2026

Benzyl chloroformate → HCID 67385303, compound

https://huagongshe.com/reaction/905950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 25068200HCID 25068200—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67385303HCID 6738530376.4%

Reaction Steps

((3R,5R)-5-Methyl-piperidin-3-yl)-carbamic acid tert-butyl ester (2.9 g, 13.53 mmol) was dissolved in 70 mL of a 1:1 mixture of dioxane and H2O and NaHCO3 (4.55 g, 54.13 mmol) was added. To the resulting suspension benzyl chloroformate (2.2 mL, 14.2 mmol) was added slowly. After 2 hours the reaction mixture was extracted with EtOAc. The combined organic layers were washed with saturated aqueous NaHCO3, dried (Na2SO4), filtered, and evaporated. The remaining oil was purified by SiO2 chromatography (150 g SiO2, hexanes/EtOAc 0 to 20% EtOAc) to give 3.6 g of (3R,5R)-3-tert-butoxycarbonylamino-5-methyl-piperidine-1-carboxylic acid benzyl ester as a colorless oil (76% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012974B2
Source datasetuspto-grants-2011_09
ORD IDord-ee91386002934f70a8f783be97eaa774
Source noteuspto-grants-2011_09