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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856772Generated: October 30, 2026

tert-Butanol → (2S,3S)-1-tert-Butoxycarbonyl-3-(2-methoxybenzyl)amino-2-phenylpiperidine

https://huagongshe.com/reaction/1856772

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantSodium HydroxideHCID 14798—
Reactant(tBuOCO)2OHCID 14215521—
ReactantCP 99994 dihydrochlorideHCID 68466923—
Product(2S,3S)-1-tert-Butoxycarbonyl-3-(2-methoxybenzyl)amino-2-phenylpiperidineHCID 11223212—

Reaction Steps

To a stirred and ice-cooled mixture of Compound 3 (10.0 g, 27.1 mmol), 3.0 M NaOH aq. (36.1 ml, 108.4 mmol) and tert-BuOH (15.0 ml) was added (tert-BuOCO)2O (Boc2O, 7.39 g, 33.8 mmol). After stirring at room temperature overnight, the mixture was extracted with AcOEt (x3). The combined AcOEt extracts were washed with sat. NaHCO3 and brine, dried over Na2SO4, and concentrated to give Compound 4 (11.3 g, quant.) as a pale yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143767
Source datasetuspto-grants-2000_11
ORD IDord-bb619cae5f0a4c1da9253b0ead3507c2
Source noteuspto-grants-2000_11