HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806784Generated: October 27, 2026
Thionyl Chloride → 4-Chloro-1-(chloromethyl)-2-methylbenzene
https://huagongshe.com/reaction/1806784
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Chloro-2-methylbenzyl Alcohol | HCID 2757669 | — |
| Product | 4-Chloro-1-(chloromethyl)-2-methylbenzene | HCID 12822618 | 93% |
Reaction Steps
Step A A mixture of 4-chloro-2-methylbenzyl alcohol (Aldrich) (5 g, 32 mmol) in thionyl chloride (20 mL) was heated at refluxing (100° C.) for 30 min. The mixture was cooled to room temperature and concentrated. The residue was diluted with ethyl acetate, washed with saturated aqueous NaHCO3 solution, water, brine, dried over MgSO4, and concentrated to give 4-chloro-2-methylbenzyl chloride as a light yellow oil (5.2 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354444B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8c4258da90734a7296f2bf2c14e81dc2 |
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| Source note | uspto-grants-2013_01 |
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