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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809931Generated: November 1, 2026

Chlorotrimethylsilane → 8-(4-Iodo-phenyl)-1,4-dioxa-spiro[4.5]decan-8-ol

https://huagongshe.com/reaction/1809931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactantp-DiiodobenzeneHCID 12208—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product8-(4-Iodo-phenyl)-1,4-dioxa-spiro[4.5]decan-8-olHCID 5780330966.6%

Reaction Steps

To a solution of 1,4-diiodobenzene (16.5 g, 50 mmol) in THF (350 mL) at −78° C. was added n-BuLi (2.5 M, 24 mL) over 1 hour. After being stirred for an additional 30 minutes, a solution of 1,4-dioxa-spiro[4.5]decan-8-one (7.8 g, 50 mmol) in THF (30 mL) was added in and the resulting mixture was stirred for 3 hours. To the mixture was added TMSCl (5.4 g, 50 mmol) and the resulting mixture was allowed to warm to rt and stirred at rt for 18 hours. The reaction mixture was neutralized to pH 6.0, and extracted with ethyl acetate (3×50 mL). The organic extracts were combined, washed with saline solution (2×50 mL), dried over sodium sulfate, concentrated in vacuo. The residue was chromatographed on silica gel, eluting with hexane/ethyl acetate (95/5 to 100/0). The appropriate fractions were combined to give 8-(4-Iodo-phenyl)-1,4-dioxa-spiro[4.5]decan-8-ol (12 g, 66.6%) with LCMS: 361.2 (M+H+, 100%) and {[8-(4-iodophenyl)-1,4-dioxaspiro[4.5]dec-8-yl]oxy}(trimethyl)silane (6 g, 27%) with LCMS: 433.1 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362003B2
Source datasetuspto-grants-2013_01
ORD IDord-c83dec9e18704492a52392cec1f47645
Source noteuspto-grants-2013_01