HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280065Generated: October 30, 2026
Ammonia → 4,8-Dimethyl-1-(p-Isopropylphenyl)-non-1-ene
https://huagongshe.com/reaction/280065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-(4,8-Dimethylnona-1,7-dien-1-yl)-4-(propan-2-yl)benzene | HCID 54431094 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,8-Dimethyl-1-(p-Isopropylphenyl)-non-1-ene | HCID 53787960 | — |
Reaction Steps
To a stirred solution of 16 g (0.7 g at) of sodium in 600 ml of liquid ammonia was added dropwise a solution of 93 g (0.34 mol.) of 4,8-dimethyl-1-(p-isopropylphenyl)nona-1,7-diene in 125 ml of anhydrous tetrahydrofuran. Total addition time was one hour. The excess sodium was destroyed by the cautious addition of methanol. Then 200 ml of hexane were added and the ammonia was allowed to evaporate. To the residue a saturated solution of NH4Cl was added cautiously. The organic layer was separated, and the aqueous layer was diluted with water and extracted twice with hexane. The combined hexane layers were washed with water, dilute HCl, brine and then dried. Evaporation of the hexane and distillation of the residue yielded the title product. Yield was 88 g (94%), bp 130°-135° C/0.1 mm. nD25 =1.4938.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE032146 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-0698b60a787a4ccb84ce57809a9bb3a8 |
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| Source note | uspto-grants-1986_05 |
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