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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403764Generated: October 30, 2026

Methanesulfonic Acid → HCID 59557745, compound

https://huagongshe.com/reaction/2403764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant(3R,4S,5R,6R)-3,4,5-Tris-trimethylsilanyloxy-6-trimethylsilanyloxymethyl-tetrahydro-pyran-2-onHCID 10994280—
ReactantHCID 59557748HCID 59557748—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventTetrahydrofuran tolueneHCID 22635083—
ProductHCID 59557745HCID 59557745—

Reaction Conditions

Temperature-65 °C

Reaction Steps

To a solution of 4-bromo-1-chloro-2-(4-(2-cyclopropoxyethyl)benzyl)benzene (105 mg, 0.29 mmol) in anhydrous toluene/THF (1.2 mL, v/v=2:1) was added dropwise n-BuLi (2.5 M in hexane, 0.14 mL) at −65° C., and the mixture was stirred for 30 min at −65° C. Then a −65° C. solution of (3R,4S,5R,6R)-3,4,5-tris(trimethylsilyloxy)-6-((trimethylsilyloxy)methyl)tetrahydro-2H-pyran-2-one (148 mg, 0.32 mmol) in toluene (1.2 mL) was added dropwise over 15 min. The mixture was stirred at −65° C. for 3 h until starting material was consumed. The reaction was quenched with methanesulfonic acid (0.04 mL, 0.60 mmol) in methanol (1 mL), and the mixture was allowed to warm to room temperature and stirred overnight. The reaction was quenched with saturated sodium bicarbonate, the organic phase was separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with saturated bicarbonate, then with water, and then with brine, and dried over sodium sulfate. Removal of the volatiles afforded a residue (134 mg), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802637B2
Source datasetuspto-grants-2014_08
ORD IDord-6922bb3cf4df4b17993475e8b169e40f
Source noteuspto-grants-2014_08