HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025772Generated: November 1, 2026
p-Diiodobenzene → 8-(4-Iodo-phenyl)-1,4-dioxa-spiro[4.5]decan-8-ol
https://huagongshe.com/reaction/1025772
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Diiodobenzene | HCID 12208 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(4-Iodo-phenyl)-1,4-dioxa-spiro[4.5]decan-8-ol | HCID 57803309 | 66.6% |
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 TMSC1 (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729063B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-0c71c70fb8614ac3868d272b406a1360 |
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| Source note | uspto-grants-2014_05 |
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