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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245593Generated: October 30, 2026

Diethyl Ether → HCID 73853093, compound

https://huagongshe.com/reaction/1245593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant4-Dodecylbenzenesulfonyl azideHCID 10915143—
Reactanttert-Butyl 4-(3-oxobutanoyl)piperidine-1-carboxylateHCID 21912749—
SolventAcetonitrileHCID 6342—
ProductHCID 73853093HCID 73853093—

Reaction Steps

A solution of 0.51 g (1.8 mmol) of 1-(tert-butoxycarbonyl)-4-(1,3-dioxo-but-1-yl)piperidine (from Step B) and 0.65 g (1.8 mmol) of para-dodecylbenzenesulfonyl azide (Syn. Comm. 1981, 11, 947–956) in CH3CN at 0° C. was treated with 0.26 mL (1.8 mmol) of triethylamine. The reaction was warmed to rt and stirred for 4.5 hours. The reaction was poured into 100 mL of Et2O and washed with 100 mL of H2O, 100 mL of 2 N HCl and 100 mL of brine. The organic layer was dried over MgSO4 and concentrated. The residue was purified with a 40M Biotage column using 9:1 v/v of hexanes/acetone to afford the title compound as a light yellow oil: RF: 0.33 (4:1 v/v hexanes/acetone); 1H-NMR (500 MHz) δ 1.46 (s, 9H), 1.57–1.76 (m, 4H), 2.42 (s, 3H), 2.82 (m, 2H), 3.24 (m, 1H), 4.14 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125887B2
Source datasetuspto-grants-2006_10
ORD IDord-986d0c6234aa46b6ad1b6a02ae87cbc8
Source noteuspto-grants-2006_10