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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743307Generated: November 3, 2026

Tert-butyl 2-{2-[(4-methylbenzenesulfonyl)oxy]ethyl}piperidine-1-carboxylate → 1-t-Butoxycarbonyl-2-(2-{2-[2-(4-ethylphenyl)ethyl]phenoxy}ethyl)piperidine

https://huagongshe.com/reaction/743307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-{2-[(4-methylbenzenesulfonyl)oxy]ethyl}piperidine-1-carboxylateHCID 15734710—
Reactant2-[2-(4-Ethylphenyl)ethyl]phenolHCID 19423998—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylacetamideHCID 31374—
Product1-t-Butoxycarbonyl-2-(2-{2-[2-(4-ethylphenyl)ethyl]phenoxy}ethyl)piperidineHCID 1942386999.3%

Reaction Steps

Following a procedure similar to that described in Example 40(a), 1.00 g of 2-[2-(4-ethylphenyl)ethyl]phenol (prepared as described in Preparation 26), 0.496 g of potassium t-butoxide and 1.70 g of 1-t-butoxycarbonyl-2-[2-(p-toluenesulfonyloxy)ethyl]piperidine were reacted in 20 ml of dimethylacetamide. The mixture was then worked up as described in Example 40(a), and the crude product thus obtained was purified by column chromatography through silica gel, using a 4:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 1.92 g (yield 99%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556864
Source datasetuspto-grants-1996_09
ORD IDord-657e56a07a3542e39d6c8423733e01af
Source noteuspto-grants-1996_09