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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534070Generated: October 30, 2026

Methanesulfonyl chloride → 1,4-Dioxaspiro[4.5]decane-2-carbimidoyl chloride

https://huagongshe.com/reaction/534070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant(R)-N-hydroxy-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chlorideHCID 86644146—
SolventTetrahydrofuranHCID 8028—
Product1,4-Dioxaspiro[4.5]decane-2-carbimidoyl chlorideHCID 8667319873.9%

Reaction Conditions

Temperature3 °C

Reaction Steps

In a 4 neck 5 L flask was added (R)-N-hydroxy-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chloride (158 g, 719 mmol) in 2.5 L of THF. The material was cooled to 3° C. and methanesulfonyl chloride (56.1 ml, 719 mmol) added in 10 mL portions over 10 minutes. N-ethyl-N-isopropylpropan-2-amine (126 ml, 719 mmol) was added through an addition funnel over 12 minutes. The reaction was stirred in an ice bath for 30 minutes and then at ambient temperature for 1 hour. The reaction was filtered and the solids washed with MTBE (3 L). The filtrate was concentrated and the residue was purified over silica gel (3 kg silica, 7:1 to 3:1 Hexane/EtOAc) to afford an oil that slowly solidified under vacuum. The solids were ground using a mortar and pestle, washed with hexanes (about 1000 mL) and dried to afford (R)-N-methylsulfonyloxy)-1,4-dioxaspiro[4.5]decane-2-carbimidoyl chloride (158 g, 531 mmol, 73.8% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853409B2
Source datasetuspto-grants-2014_10
ORD IDord-e4a40d9837984bd593317b7ca0bb808e
Source noteuspto-grants-2014_10