HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701239Generated: October 30, 2026
Iodine → (2R,6R)-(+)-1-tert. Butoxy-2,6,10-trimethylundecane
https://huagongshe.com/reaction/1701239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | (R)-1-bromo-3,7-dimethyloctane | HCID 12801557 | — |
| Reactant | (S)-(+)-3-tert. butoxy-2-methyl-1-propyl p-toluenesulfonate | HCID 86735106 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R,6R)-(+)-1-tert. Butoxy-2,6,10-trimethylundecane | HCID 12923314 | — |
Reaction Steps
A mixture of 2.33 g. (0.097 mole) of powdered magnesium and a few iodine crystals in 23 ml. of dry tetrahydrofuran was stirred at reflux temperature while a solution of 17.9 g. (0.08 mole) of (R)-(-)-1-bromo-3,7-dimethyloctane in 51 ml. of dry tetrahydrofuran was added dropwise over 1 hour. The mixture was stirred at reflux for an additional 1 hour then cooled to room temperature. To a solution of 19.5 g. (0.065 mole) of (S)-(+)-3-tert. butoxy-2-methyl-1-propyl p-toluenesulfonate in 56 ml. of dry tetrahydrofuran, stirring at -78° C. was added the R-3,7-dimethyl-1-octyl magnesium bromide solution dropwise, followed by 3.3 ml. of a 0.1 M Li2CuCl4 solution in dry tetrahydrofuran. The resulting mixture was stirred at -78° C. for 10 minutes, for 2 hours at 0°-5° C. (ice bath) and finally for 18 hours at room temperature. At the end of this time, the reaction mixture was treated with 1 N aqueous H2SO4 and work up was carried out by extraction with ether in the manner of Example 1. The crude product was chromatographed on 450 g. of silica gel. Elution with 19:1 parts by volume hexane-ether gave the desired product which was distilled under high vacuum yielding 12.5 g. of (2R,6R)-(+)-1-tert. butoxy-2,6,10-trimethylundecane as a colorless oil, b.p. 91°-95° C. (0.3 mm Hg); [α]25D+0.94° (c 2.01, hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04191842 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-34e94312258449aeba66cb6a79ff15db |
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| Source note | uspto-grants-1980_03 |
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