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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14455Generated: October 27, 2026

Borane;tetrahydrofuran → (R)-2-Bromo-1-(2,2-dimethyl4H-benzo[1,3]dioxin-6-yl)ethanol

https://huagongshe.com/reaction/14455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantEthanone, 2-bromo-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-HCID 11150315—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-Bromo-1-(2,2-dimethyl4H-benzo[1,3]dioxin-6-yl)ethanolHCID 25098927—

Reaction Steps

To the product of step (c) (10 g, 35.1 mmol) in 100 mL of THF was added the solid catalyst of Preparation 13, step (c)(1) (0.97 g, 3.5 mmol). The solution was cooled to between −20° C. and −10° C. and BH3-THF (35 mL, 35 mmol) diluted with 50 mL THF was added dropwise via a dropping funnel. After the addition was complete, the reaction mixture was allowed to warm to ambient temperature. After 30 minutes, the reaction mixture was quenched by slow addition of 50 mL of methanol and then concentrated to a thick oil. The oil was purified by silica gel chromatography eluted with 1:2 ethyl acetate/hexanes. The fractions were combined and concentrated to give the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732441B2
Source datasetuspto-grants-2010_06
ORD IDord-b4561e27a48a4ac2be01e25b255a31a5
Source noteuspto-grants-2010_06