HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Chloro-5,5-dimethylnonan-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | 2-Chloro-2-methylhexane | HCID 138224 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178443943 | HCID 178443943 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Chloro-5,5-dimethylnonan-4-one | HCID 20386073 | — |
Reaction Steps
Four hundred ml. of a solution in ether of 1,1-dimethylpentylmagnesium chloride prepared from magnesium (24.3 g., 1.0 mole) and 1-chloro-1,1-dimethylpentane (134.5 g., 1.0 mole) according to the procedure of Whitmore and Badertscher [J. Am. Chem. Soc., 55, 1559 (1933)] is added dropwise with stirring to 4-chlorobutyryl chloride (197 g., 1.4 moles) in ether (400 ml.) during 6 hours. The reaction mixture is stirred for an additional 12 hours. It is then poured into a mixture of ice and dilute hydrochloric acid. The ether layer is separated, washed with water and brine and dried over sodium sulfate. The ether is evaporated and the residue distilled at aspirator vacuum through a Vigreaux column to yield the product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055597 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-81f2ed12d2ff4899a12f74c1d2efa295 |
| Source note | uspto-grants-1977_10 |