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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118314Generated: November 1, 2026

Hydrochloric Acid → (1R)-2-Azido-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanol

https://huagongshe.com/reaction/2118314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant2-Azido-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanoneHCID 11402365—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(1R)-2-Azido-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanolHCID 8659526068.2%

Reaction Steps

R-(+)-2-Methyl-CBS-oxazaborolidine solution in toluene (1M, 7.5 ml) was added to THF (75 ml) and the solution was diluted to 0° C. Borane-THF complex (1M solution in THF, 125 ml) was added and the mixture was stirred under nitrogen for 15 min. A solution of 2-azido-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)ethanone (24.7 g) in THF (250 ml) was added dropwise over 1.5 h at 5° C. The mixture was stirred for a further 1 h and then cautiously treated with 2M HCl (100 ml). The reaction mixture was extracted with ether and the organic layer was washed with 2M HCl, NaHCO3, brine, dried (MgSO4). The solvent was removed by evaporation and the residue was chromatographed on a Biotage column eluting with diethyl ether-petrol (40-60° C.) (1:9; 1:1) to give the title compound (16.99 g). ES+ve 250 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442837B2
Source datasetuspto-grants-2008_10
ORD IDord-c77daf7d4ad549b2a87efcd06417ad02
Source noteuspto-grants-2008_10