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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629841Generated: October 25, 2026

Hydrochloric Acid → 873806-20-3

https://huagongshe.com/reaction/629841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178462446HCID 178462446—
SolventTetrahydrofuranHCID 8028—
Product873806-20-3HCID 12171955—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of Ia (7.0 g, 50 mmol) in dry THF (25 mL) at −78° C. was added n-BuLi (1.6 M in n-hexane, 62.5 mL, 100 mmol). After being stirred for 1 hour at −78° C., the reaction mixture was warmed to room temperature and stirred for 1 hour at that temperature. Another flask was charged with 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (7.8 mL, 38 mmol) in dry THF (50 mL) under argon atmosphere, and the reaction mixture was cooled to −78° C. The lithium acetylide from the first flask, which was cooled to −78° C., was slowly added to the second by a double-ended needle. The mixture was stirred at −78° C. for 2 hours, after which anhydrous HCl (100 mmol) was added. Then, reaction mixture was warmed to room temperature. After removal of the precipitated LiCl by filtration and removal of solvents under reduced pressure, the residue was purified by distillation (113-115° C./7 mbar) to afford IIIa (5.9 g, 80%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315525B2
Source datasetuspto-grants-2016_04
ORD IDord-d0388a5d128947039f58c65e1a47e386
Source noteuspto-grants-2016_04