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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366516Generated: October 31, 2026

Cesium carbonate → tert-Butyl 2-(but-3-yn-1-yl)-2,9-diazaspiro[5.5]undecane-9-carboxylate

https://huagongshe.com/reaction/2366516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-Bromobut-1-yneHCID 11073464—
ReactantTert-butyl 2,9-diazaspiro[5.5]undecane-9-carboxylate hydrochlorideHCID 71464197—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 2-(but-3-yn-1-yl)-2,9-diazaspiro[5.5]undecane-9-carboxylateHCID 8670185998%

Reaction Steps

Cesium carbonate (46.66 g, 143.21 mmol) is added to a suspension of tert-butyl 4,9-diazaspiro[5.5]undecane-9-carboxylate hydrochloride (16.66 g, 57.28 mmoles) in acetonitrile (167 mL). The mixture is stirred for 10 minutes at ambient temperature then 4-bromobutyne (6.45 mL, 68.74 mmol) is added. The reaction is heated to reflux and stirred for 18 hours. The mixture is cooled and concentrated under reduced pressure. The residue is partitioned between water (200 mL) and ethyl acetate (150 mL). The phases are separated and the aqueous layer is extracted with ethyl acetate (100 mL). The combined organic layers are washed with water (200 mL), then brine (150 mL), dried over MgSO4, filtered, and concentrated under reduced pressure to give the title compound (17.2 g, 98% yield). 1H NMR (300.11 MHz, CDCl3): δ 3.43-3.31 (m, 4H), 2.53-2.48 (m, 2H), 2.37-2.29 (m, 4H), 2.20 (s, 2H), 1.94 (t, J=2.6 Hz, 1H), 1.44 (s, 17H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697849B2
Source datasetuspto-grants-2014_04
ORD IDord-1a43b68cb04f4d13a829944c1ab65160
Source noteuspto-grants-2014_04