HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111643Generated: October 28, 2026
1,3-Dichlorobenzene → HCID 20315348, compound
https://huagongshe.com/reaction/1111643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dichlorobenzene | HCID 10943 | — |
| Reactant | 2-Butyloxirane | HCID 15036 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 20315348 | HCID 20315348 | — |
Reaction Steps
A slurry of m-dichlorobenzene, 735 g. (5.0 mole) and anhydrous aluminium chloride, 162 g. (1.1 mole) is cooled to 10° using an ice-water bath and 1,2-epoxyhexane, 100 g. (1.0 mole) is added dropwise over a one hour period. The temperature of the reaction is kept below 15°. The reaction mixture is allowed to come to room temperature and stirring is continued overnight. The reaction mixture is then poured into a 4 liter flask containing ice and concentrated hydrochloric acid (50 ml.) with stirring. The aqueous and organic layers are separated and the aqueous layer extracted three times with ether (150 ml). The combined organic extracts are washed twice with water (50 ml) and dried over magnesium sulfate. Solvent is evaporated and vacuum distillation (160°-172°/0.1 mm) gives 114 g. (46%) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04118461 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-d7f4652c08934627ad2ea49c16584f40 |
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| Source note | uspto-grants-1978_10 |
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