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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094632Generated: November 1, 2026

Tetrahydrofuran → HCID 178462213, compound

https://huagongshe.com/reaction/1094632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant(R)-t-butylsulfinylamideHCID 86609349—
ReactantHCID 178466050HCID 178466050—
CatalystTitanium tetraethoxideHCID 76524—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178462213HCID 178462213—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a THF (25 ml) solution of 1-(1H-1,2,3-benzotriazol-6-yl)ethanone (1.85 g, 11.5 mmol), (R)-(+)-2-methyl-2-propanesulfinylamide (2.30 g, 18.9 mmol) and titanium(IV) ethoxide (25 ml) were added and the mixture was stirred for 24 hours at 70° C. Then, the mixture was cooled to 0° C. and sodium borohydride (1.5 mg, 40 mmol) was added. After stirring for 2 hours, water and EtOH were added to the mixture with stirring for 1 hour at room temperature. Filtration, evaporation gave N-[(1R)-1-(1H-1,2,3-benzotriazol-6-yl)ethyl]-2-methylpropane-2-sulfinamide (99% d.e.) (MS (ESI) m/z 265 (M−H)−, 267 (M+H)+) which was treated with hydrochloric acid-MeOH (2.0 M, 15.0 ml) and 1,4-dioxane (15.0 ml) for 1.5 hours at room temperature. Then, the reaction mixture was evaporated and diethyl ether was added to form a precipitate, which was collected, washed with diethyl ether to give 1.26 g (68%) of the title compound. MS (ESI) m/z 161 (M−H)−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134004B2
Source datasetuspto-grants-2012_03
ORD IDord-45e0aa29cafa4fd8aa369240598d1bfe
Source noteuspto-grants-2012_03