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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332659Generated: October 25, 2026

Aluminium lithium hydride → (3-((8-(1,3-Dioxolan-2-yl)octyl)oxy)-5-bromophenyl)methanol

https://huagongshe.com/reaction/332659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantBenzyl 3-((8-(1,3-dioxolan-2-yl)octyl)oxy)-5-bromobenzoateHCID 71093165—
SolventTetrahydrofuranHCID 8028—
Product(3-((8-(1,3-Dioxolan-2-yl)octyl)oxy)-5-bromophenyl)methanolHCID 71093288—

Reaction Steps

To a solution of benzyl 3-((8-(1,3-dioxolan-2-yl)octyl)oxy)-5-bromobenzoate in tetrahydrofuran (30 mL) at −78° C., was added a solution of lithium aluminium hydride in THF (2.0 M, 3.3 mL, 6.60 mmol). The reaction mixture was stirred for 4 hours, then quenched with water (0.25 mL), 2 M sodium hydroxide (0.25 mL) and water (0.75 mL). The coolant was removed and ethyl acetate and magnesium sulphate was added, and the mixture stirred at room temperature for 20 minutes. The suspension was filtered, washed with ethyl acetate, and the filtrate was concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 0-17% ethyl acetate in iso-hexane to afford the title compound as a 10:7 ratio of product to starting material (1.69 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877774B2
Source datasetuspto-grants-2014_11
ORD IDord-e554c44202804fbfb7fbcdb4b1c0e0ba
Source noteuspto-grants-2014_11