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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451662Generated: October 26, 2026

Red-Al → (R)-tert-butyl 3-((R)-(2-aminoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/451662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRed-AlHCID 16684438—
Reactant(R)-tert-butyl 3-((R)-(2-amino-2-oxoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylateHCID 59598485—
SolventTolueneHCID 1140—
Product(R)-tert-butyl 3-((R)-(2-aminoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylateHCID 59598469109.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(R)-tert-butyl 3-((R)-(2-amino-2-oxoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate (1.10 g, 2.60 mmol) was dissolved in anhydrous toluene (30 mL) and cooled to 0° C. Red-Al (65% in toluene, 2.6 mL, 8.64 mmol) was added dropwise. After the addition, the reaction was stirred at rt for 12 h and quenched by adding water slowly. The resulting mixture was filtered through Celite and washing with THF. The filtrate was evaporated under reduced pressure to give crude product 1.05 g. It was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-ba36621c921544d6a72ece6accfa3f07
Source noteuspto-grants-2013_07