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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842209Generated: November 2, 2026

1,3-Dithiane → HCID 12102453, compound

https://huagongshe.com/reaction/1842209

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DithianeHCID 10451—
Reactant(-)-Benzyl (R)-glycidyl etherHCID 159746—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12102453HCID 1210245384.9%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution containing 1,3-dithiane (11 g) in THF (190 mL) was cooled to −70° C. n-Butyllithium (2.64 M solution in hexane, 35 mL) was added to the reaction solution, and then the mixture was heated to −30° C. and stirred for one hour. The reaction solution was cooled to −70° C., and a solution containing benzyl (R)-(−)-glycidyl ether (16.5 g) in THF (18 mL) was added dropwise. The cooling bath was removed and the mixture was gradually warmed to room temperature. After stirring overnight, a saturated ammonium chloride solution, brine and t-butyl methyl ether were added to the reaction solution, and the organic layer was separated. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration and then the filtrate was concentrated under reduced pressure to obtain a residue. The residue was subjected to silica gel column chromatography to obtain the title compound (22.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946210B2
Source datasetuspto-grants-2015_02
ORD IDord-360d68c1a4804ce293d82e412040a660
Source noteuspto-grants-2015_02