HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846714Generated: October 31, 2026
4-Chlorobenzoyl chloride → HCID 19883675, compound
https://huagongshe.com/reaction/846714
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | 7-Phenyl-1-heptyl chloride | HCID 522410 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | HCID 19883675 | HCID 19883675 | 74.4% |
Reaction Steps
1.07 g of 7-chloroheptylbenzene and 0.89 g of 4-chlorobenzoyl chloride were dissolved in 10 ml of nitrobenzene and treated with 0.82 g of aluminium chloride under argon and while cooling with ice. The mixture was then stirred at room temperature for 18 hours, taken up in 100 ml of ice-cold 2N hydrochloric acid solution and extracted three times with 50 ml of ether each time. The organic phases were washed with 50 ml of a 10 percent sodium bicarbonate solution and 50 ml of a saturated sodium chloride solution, dried over magnesium sulphate and concentrated. The nitrobenzene was removed by distillation at 80°-100° C. and 20 Pa. By distillation at 240°-250° C. and about 13.4 Pa there were obtained 1.32 g (74%) of 4-chloro-4'-(7-chloroheptyl)benzophenone as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05137920 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-186bfe639a67481aae1a7daa1a88b54e |
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| Source note | uspto-grants-1992_08 |
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