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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849765Generated: October 31, 2026

1,4-Dioxaspiro(4.5)decan-8-ol → Tert-butyl 4-(1,4-dioxaspiro[4.5]decan-8-yloxy)-5-chloro-2-fluorobenzoate

https://huagongshe.com/reaction/1849765

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxaspiro(4.5)decan-8-olHCID 567352—
ReactantPotassium tert-butoxideHCID 23665647—
Reactanttert-butyl 5-chloro-2,4-difluorobenzoateHCID 58042499—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 4-(1,4-dioxaspiro[4.5]decan-8-yloxy)-5-chloro-2-fluorobenzoateHCID 8670364912.1%

Reaction Steps

To a mixture of 1,4-dioxaspiro[4.5]decan-8-ol (2.40 g, 15.20 mmol) and tert-butyl 5-chloro-2,4-difluorobenzoate (3.78 g, 15.20 mmol) in anhydrous dimethyl sulfoxide was added potassium tert-butoxide (2.56 g, 22.80 mmol) and the reaction mixture was stirred for 16 hours at ambient temperature. After dilution with ethyl acetate (200 mL), the organic phase was washed with water (3×10 mL), brine (10 mL), and dried over anhydrous sodium sulfate. Filtration and concentration of the filtrate under reduced pressure gave a residue which was purified by silica gel column chromatography using 0-30% ethyl acetate in hexanes as eluent to afford the title compound as a colorless oil (0.709 g, 12%): 1H NMR (300 MHz, CDCl3) δ 7.85 (d, J=7.8 Hz, 1H), 6.64 (d, J=12.3 Hz, 1H), 4.53-4.46 (m, 1H), 3.97-3.92 (m, 4H), 2.04-1.58 (m, 8H), 1.55 (d, J=1.0 Hz, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-89ae82330eb14f6aae44f965e060c6e0
Source noteuspto-grants-2015_02