HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978160Generated: October 30, 2026
Benzyl Chloride → 3,4-Dichlorophenyl benzyl carbinol
https://huagongshe.com/reaction/978160
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3,4-Dichlorophenyl benzyl carbinol | HCID 19852792 | 96.8% |
Reaction Steps
Into a 1000 ml three necked flask equiped with a reflux condenser and an addition funnel was placed 8.8 g of magnesium turnings (0.36 mole) and 400 ml of diethyl ether. After activation of the magnesium with 0.02 g of iodine, the mixture was heated to reflux and a solution of 44 g (0.35 mole) of benzyl chloride in ethyl ether was added at a rate to maintain the reflux. When the reaction had subsided, a solution of 50 g (0.29 mole) of 3,4-dichlorobenzaldehyde in 75 ml of diethyl ether was added at a rate to maintain reflux. After 15 minutes, the reaction was quenched with water and acidified with dilute hydrochloric acid. The organic layer was washed with brine, dried, and concentrated in vacuo yielding 75 g of 3,4-dichlorophenyl benzyl carbinol which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663341 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-4073f7222cbe42aaaddf7e1a97cbf864 |
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| Source note | uspto-grants-1987_05 |
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