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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225359Generated: October 25, 2026

Iodine → 4,4-Dimethyl-1-iodo-trans-1-octen-3-ol

https://huagongshe.com/reaction/225359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantEthanamine, N,N-diethyl-, N-oxideHCID 123168—
ReactantBis(1,2-dimethylpropyl)boraneHCID 192733—
Reactant2-[(4,4-Dimethyloct-1-YN-3-YL)oxy]oxaneHCID 14516370—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventDiglymeHCID 8150—
Product4,4-Dimethyl-1-iodo-trans-1-octen-3-olHCID 20465723—

Reaction Steps

To 233 ml. of a 0.43N solution of disiamylborane in diglyme cooled to 0° C. under an inert atmosphere is added 23.8 g. (0.100 mole) 4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne (Example 150). The mixture is allowed to come to room temperature and is stirred at ambient temperature for 3 hours. The solution is cooled to 0° C. and 22.5 g. (0.30 mole) of triethylamine oxide is added portionwise such that the temperature is maintained at 0°-5° C. The mixture is stirred at 0° C. for 1 hour and is then poured into 150 ml. of 1N sodium hydroxide followed immediately by a solution of 25.4 g. (0.100 mole) of iodine in 60 ml. of tetrahydrofuran. The mixture is stirred at ambient temperatures for 0.5 hour and poured into 500 ml. of water. The mixture is decolorized by addition of sodium thiosulfate and is extracted into ether. The organic phase is washed with water and the solvent is removed in vacuo. The residue is stirred at room temperature for 20 hours with 900 ml. 3:1:1 tetrahydrofuran-acetic acid-water. The solution is evaporated in vacuo and the residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04236027
Source datasetuspto-grants-1980_11
ORD IDord-b3ed1c5eb7ec458da278158e2c62ca38
Source noteuspto-grants-1980_11