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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963943Generated: November 1, 2026

Methanesulfonyl chloride → HCID 86650639, compound

https://huagongshe.com/reaction/1963943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(6,6-Dimethyl-1,4-dioxan-2-yl)methanolHCID 66937181—
SolventDichloromethaneHCID 6344—
ProductHCID 86650639HCID 8665063998%

Reaction Steps

TEA (0.52 mL, 3.74 mmol) and (6,6-dimethyl-1,4-dioxan-2-yl)methanol (390 mg, 2.67 mmol) were dissolved in DCM (10 mL). Methanesulfonyl chloride (0.249 mL, 3.20 mmol) was slowly added at 0° C. After the addition was completed the solution was warmed to ambient temperature and stirred for 1 hr. Saturated NaHCO3 solution was added and the two layers were separated. The aqueous layer was extracted three times with DCM. The organic layers were combined, dried over Na2SO4 and concentrated. The resulting residue was purified on a silica gel column (heptane:EtOAc 4:1 to 1:1) to give the product as a colorless oil (584 mg, 98%). 1H NMR (400 MHz, CDCl3) δ ppm 4.00-4.09 (3H, m), 3.74 (1H, dd, J= 11.2, 2.8 Hz), 3.42 (1H, d, J= 11.6 Hz), 3.16-3.23 (2H, m), 2.99 (3H, s), 1.27 (3H, s), 1.05 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415381B2
Source datasetuspto-grants-2013_04
ORD IDord-77afdf421cf244fd931e5da4650af7b0
Source noteuspto-grants-2013_04