HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 3-(Tert-butoxy)-1-iodohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | 1-Iodohexan-3-OL | HCID 18921004 | — |
| Reactant | 1-Chlorohexan-3-ol | HCID 18921007 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 3-(Tert-butoxy)-1-iodohexane | HCID 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, containing 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; μ max. 7.22 and 7.37 μ (tert-butyl group).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007210 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-1fd9f8979d5048e9b341418b4ae957f4 |
| Source note | uspto-grants-1977_02 |