HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Heptylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Heptylbenzoic acid | HCID 18417671 | — |
| Product | Heptylbenzoyl chloride | HCID 22920781 | 80% |
Reaction Steps
Heptylbenzoyl chloride (530 mg., 0.0022 M), obtained by reaction of heptylbenzoic acid with SOCl2, and 380 mg. of ##STR15## (0.002 M) in 5 ml. of pyridine are allowed to react at ambient temperature for 48 hours. Then the reaction mixture is poured into a solution of 5 ml. of concentrated H2SO4 and 50 g. of ice. The organic fraction is extracted with ether (3 times, 100 ml. total). The organic fraction is washed with water (3 times) and dried over anhydrous Na2SO4. The solvent is evaporated and the solid residue is treated by chromatography on silica with a benzene (50%) hexane (50%) mixture. The product is finally recrystallized twice from ethanol. The yield is above 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04147655 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-d2d113151734485182f3aa6cb97be9e5 |
| Source note | uspto-grants-1979_04 |