HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167885Generated: October 25, 2026
Hydrochloric Acid → (2-Chloro-4-methylphenyl)methanol
https://huagongshe.com/reaction/2167885
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 2-Chloro-4-methylbenzoic acid | HCID 2735755 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Chloro-4-methylphenyl)methanol | HCID 15544016 | 89.8% |
Reaction Steps
as follows: To a solution of 2-chloro-4-methylbenzoic acid (2.18 g; 12.8 mmol) in THF (22 mL) was added dropwise a solution of BH3.THF in THF (25.6 ml; 1.00 mol/l; 25.6 mmol), at 0° C. Upon complete addition the resulting mixture was heated under reflux, for 3 hours. Subsequently, the mixture was cooled to 0° C., 1M aqueous HCl (30 mL) was added dropwise, and the mixture was stirred for 10 min. Et2O (100 mL) was added and the layers were separated. The organic layer was washed with 1M aqueous HCl (2×), 5% aqueous NaHCO3 (2×), and brine, dried (Na2SO4), filtered and concentrated in vacuo to afford (2-chloro-4-methyl-phenyl)-methanol (1.80 g), which was used as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045441B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-50db0fbaaa8e4b968395e9a42dc1411a |
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| Source note | uspto-grants-2015_06 |
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