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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249883Generated: October 27, 2026

Methanesulfonyl chloride → 1,4-Dioxaspiro[4.5]decan-8-ylmethyl methanesulfonate

https://huagongshe.com/reaction/2249883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,4-Dioxaspiro[4.5]decan-8-ylmethanolHCID 10080838—
SolventDichloromethaneHCID 6344—
Product1,4-Dioxaspiro[4.5]decan-8-ylmethyl methanesulfonateHCID 9992301—

Reaction Steps

To a solution of (1,4-dioxa-spiro[4.5]dec-8-yl)-methanol (1.0 g, 5.8 mmol, 1.0 eq.) and ethyldiisopropylamine (17 mL, 3.0 eq.) in methylene chloride (4 mL) at 0° C. was added dropwise MsCl (0.46 mL, 1.0 eq.) and the resulting mixture was warmed to room temperature and stirred for 2 h. The reaction was quenched by addition of sat. NaHCO3 and the separated aqueous phase was extracted with 3× methylene chloride and 4×EtOAc. The combined organic phase was dried over over Na2SO4, filtered and concentrated to give a crude methanesulfonic acid 1,4-dioxa-spiro[4.5]dec-8-ylmethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314936B2
Source datasetuspto-grants-2008_01
ORD IDord-71b6be571e9c4f57bff380caf9e947ce
Source noteuspto-grants-2008_01