HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872805Generated: November 1, 2026
Hydrochloric Acid → 1-Bromo-12-methyltridecane
https://huagongshe.com/reaction/1872805
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | 1,10-Dibromodecane | HCID 221483 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Copper;dilithium;tetrachloride | HCID 193501 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Bromo-12-methyltridecane | HCID 11065733 | 33.1% |
Reaction Steps
Isobutyl bromide (27.4 g) was added to magnesium (5.0 g) in tetrahydrofuran (100 ml). The mixture was stirred for 1 hour under nitrogen atmosphere. The mixture was added to a solution of 1,10-dibromodecane (50.0 g) and dilithium tetrachlorocuprate (1 m mole) in tetrahydrofuran (100 ml) at 0° C. under nitrogen atmosphere. The mixture was stirred at 0° C. for 1 hour and poured into a mixture of 7% hydrochloric acid (200 ml) and ethyl acetate (200 ml). The organic layer was washed with water, dried over magnesium sulfate and evaporated. The residue was distilled under reduced pressure to give a mixture of the product and 1,10-dibromodecane as a colorless oil (27.23 g) (bp.115-120° C./0.5 Torr). The mixture was chromatographed on a silica gel column eluting with n-hexane to give 1-bromo-12-methyltridecane as an oil (15.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06110933 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-a93cf02c5cee410387ce3a86be2e5273 |
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| Source note | uspto-grants-2000_08 |
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