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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171828Generated: November 1, 2026

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

https://huagongshe.com/reaction/1171828

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 numberUS07829583B2
Source datasetuspto-grants-2010_11
ORD IDord-e9efd836b17f4f8eb03249e5c2e89b50
Source noteuspto-grants-2010_11