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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112673Generated: October 31, 2026

Sulfuric Acid → 3-(Tert-butoxy)-1-iodohexane

https://huagongshe.com/reaction/1112673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium IodideHCID 5238—
ReactantIsobutyleneHCID 8255—
Reactant1-Iodohexan-3-OLHCID 18921004—
Reactant1-Chlorohexan-3-olHCID 18921007—
SolventDichloromethaneHCID 6344—
SolventMethyl Ethyl KetoneHCID 6569—
Product3-(Tert-butoxy)-1-iodohexaneHCID 20465618—

Reaction Steps

A mixture of 23.4 g. of 1-chloro-3-hexanol [Fourneau, et. al., Bull. Soc. Chem. France, 25, 367 (1919)] in 300 ml. of 2-butanone containing 30 g. of sodium iodide is stirred at the reflux temperature for 18 hours. The cooled solution is filtered and the mother liquor is taken to dryness. Distillation of the residue affords 32.9 g. (84%) of 1-iodo-3-hexanol, b.p. 105° C. (10 mm). Treatment of this material in 500 ml. of methylene chloride, contaning 4 ml. of concentrated sulfuric acid, with isobutylene according to the procedure described in Example 492 gives 27 g. of crude material. Chromatography on florisil affords 16 g. of product; λmax. 7.22 and 7.37 μ (tert-butyl group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123456
Source datasetuspto-grants-1978_10
ORD IDord-79e8c10866214464a828751c275f414f
Source noteuspto-grants-1978_10