HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Propylhept-1-en-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Heptanone | HCID 31246 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Propylhept-1-en-4-ol | HCID 551382 | — |
Reaction Steps
113 g of 4-heptanone in 1000 ml of dry diethyl ether was slowly added to a solution of allylmagnesium bromide, prepared from 36.5 g of Mg and 178 g of allyl bromide in 500 ml dry diethyl ether. After the addition the mixture was refluxed for 10 hrs. The reaction mixture was poured on a mixture of 150 g ice, 450 ml of 20% NH4Cl and 350 ml of 5M HCl. The ether phase was separated and the water phase extracted with diethyl ether (3×100 ml). The combined organic phases were then washed with a Na2CO3 -solution and water, dried with Na2SO4 and evaporated. The residue was distilled. Yield: 142 g (b.p. 38°-40° C./0.1 torr) 1H-NMR(CDCl3): δ0.9(6H,CH3), 1.3-1.6(9H,CH2,OH), 2.1-2.3 (CH2C=C), 5.0-5.2(CH2 =C), 5.6-6.1 (CH=C)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155220 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-a3d205f1e1574d3a8469185ccbac3dce |
| Source note | uspto-grants-1992_10 |