Triethylamine → Oxan-4-ylmethyl methanesulfonate

Temperature

0 °C

A solution of 90 g (774.8 mmol) of tetrahydropyran-4-methanol and 129.6 mL (929.76 mmol, 1.2 eq.) of triethylamine in 775 mL of anhydrous DCM was cooled to 0° C. with in an ice bath. Methanesulfonyl chloride (66.2 mL, 852.28 mmol, 1.1 eq.) of was then added dropwise over 60 minutes while maintaining the temperature around 0° C. The reaction mixture was stirred for 30 minutes at 0° C. and quenched with a saturated solution of sodium bicarbonate (800 mL). The aqueous layer was extracted with DCM (800 mL). The combined organic layers were washed with water (2×800 mL), brine (800 mL) and dried over sodium sulfate. After filtration and concentration in vacuo, a yellowish solid (146.1 g, 97%) was obtained corresponding to the methanesulfonic acid tetrahydropyran-4-ylmethyl ester.

1. customquenched with a saturated solution of sodium bicarbonate (800 mL)
2. extractionThe aqueous layer was extracted with DCM (800 mL)
3. washThe combined organic layers were washed with water (2×800 mL), brine (800 mL)
4. dry with materialdried over sodium sulfate
5. filtrationAfter filtration and concentration in vacuo

ORD record

ord-14dcb94d9d554dc1a53f6ef977427d61

Source dataset

uspto-grants-2012_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08124613B2