HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659821Generated: November 1, 2026
Triphenylphosphine → (R)-1-bromo-3,7-dimethyloctane
https://huagongshe.com/reaction/1659821
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (3R)-3,7-Dimethyl-1-octanol | HCID 6999991 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-1-bromo-3,7-dimethyloctane | HCID 12801557 | 87.3% |
Reaction Steps
5.65 g (31.8 mmol) of N-bromosuccinimide are added portionwise while stirring to a solution of 5 g (31.6 mmol) of (R)-3,7-dimethyl-1-octanol and 9.05 g (34.5 mmol) of triphenylphosphine in 20 ml of methylene chloride. The temperature is held below 25° by occasional cooling of the reaction vessel. After 30-minutes stirring at room temperature, the solvent is removed on the rotary evaporator. The residue is washed out several times with n-hexane, then filtered and again rinsed with n-hexane. The combined n-hexane phases are concentrated on the rotary evaporator and the crude product is chromatographed on 200 g of silicagel with n-hexane. Distillation in the bulb-tube at 105°/15 Torr gives 6.1 g (87%) of (R)-1-bromo-3,7-dimethyloctane; [α]D20 =-5.0 (c=0.82, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04305876 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-b3df32d7a6e04c08a873e2c0b43c7ccd |
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| Source note | uspto-grants-1981_12 |
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