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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915716Generated: October 31, 2026

Sodium Thiosulfate → tert-Butyl 4-(2-oxoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/915716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
ReactantTempoHCID 2724126—
ReactantIodo benzene diacetateHCID 12217721—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(2-oxoethyl)piperidine-1-carboxylateHCID 10353694—

Reaction Steps

To a flask containing tert-butyl 4-(2 hydroxyethyl)piperidine-1-carboxylate (4.4 g, 19.2 mmol) in CH2Cl2 (20 mL) was added TEMPO (300 mg, 1.92 mmol) followed by iodobenzene diacetate (6.8 g, 21.1 mmol). The reaction was stirred 3 hours and then diluted with CH2Cl2 (100 mL). Saturated aqueous solution of Na2S2O3 (100 mL) was added and extracted with CH2Cl2 (3×50 mL). The combined organics were washed with saturated aqueous NaHCO3 (150 mL) and brine (150 mL), dried over Na2SO4, and concentrated in vacuo. The resulting residue was purified by silica gel chromatography (40-70% Et2O/pentanes) to provide the title compound, which was identical to the reported literature compound (see Sato et al. (2001) Heterocycle 54: 747). 13C NMR (75 MHz, CDCl3) δ 201.5, 154.7, 79.4, 50.3, 43.7, 31.9, 30.6, 28.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265249B2
Source datasetuspto-grants-2007_09
ORD IDord-1d8544f64d794995bd473023db2d87b3
Source noteuspto-grants-2007_09