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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107051Generated: October 26, 2026

Water → (2S)-2-((1-Naphthalenyloxy)methyl)oxirane

https://huagongshe.com/reaction/1107051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-NaphtholHCID 7005—
ReactantCesium fluorideHCID 25953—
ReactantBenzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl esterHCID 146490—
SolventDimethylformamideHCID 6228—
Product(2S)-2-((1-Naphthalenyloxy)methyl)oxiraneHCID 14893396.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Naphthol (1.0 g) was dissolved in DMF (8 ml) under nitrogen atmosphere and the solution was cooled to 0° C. 25 Cesium fluoride (2.1 g) was added thereto and the mixture was stirred for 1 hour. Then, (S)-glycidyl m-nitrobenzenesulfonate (1.80 g, 99.3% e.e.) was added thereto and the mixture was stirred for 24 hours at the same temperature. After the reaction water was added to the mixture, the mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, condensed and the residue was subjected to silica gel chromatography (hexane/ethyl acetate; 6:1) to give 1.34 g of (S)-1-(2,3-epoxypropoxy)naphthalene (yield 96.5%, optical purity 99.2% e.e.) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057476
Source datasetuspto-grants-2000_05
ORD IDord-a0d145534f774bbab6d2e72ab5b3b57f
Source noteuspto-grants-2000_05