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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449498Generated: October 26, 2026

2-Chlormethyl-8-(1,1-dimethylethyl)-1,4-dioxaspiro(4.5)decan → 8-t-Butyl-2-(phthalimidomethyl)-1,4-dioxaspiro(4,5)decane

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Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlormethyl-8-(1,1-dimethylethyl)-1,4-dioxaspiro(4.5)decanHCID 14326294—
ReactantPhthalimide potassium saltHCID 24194345—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
Product8-t-Butyl-2-(phthalimidomethyl)-1,4-dioxaspiro(4,5)decaneHCID 19963664101.4%

Reaction Steps

A mixture of 8-t-butyl-2-chloromethyl-1,4-dioxaspiro(4,5)decane (10 g, 40 mmol) (prepared as described in EP 281842; see also the references cited in this document for-related compounds), potassium phthalimide (8.9 g, 48 mmol) and a catalytic amount of tetra-n-butyl ammonium iodide in DMF (80 ml) were heated to 120° C. for 3 hours. Additional potassium phthalimide (2.8 g, 16 mmol) was then added and heating was continued for 6 hours. The solvent was then evaporated in vacuo and toluene (150 ml) was added. After filtration from insoluble material the organic phase was washed two times with brine (100 ml), dried (MgSO4) and evaporated in vacuo. The resulting residue (22 g) was purified by flash chromatography on silica (toluene/ethylacetate 3:1) yielding the title compound as light yellow crystals (14.5 g, Fp. 97°-115° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599818
Source datasetuspto-grants-1997_02
ORD IDord-f51cbe3ec0384ca0868a54b86681f1cb
Source noteuspto-grants-1997_02