HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602586Generated: October 27, 2026
Lithium iodide → 3-Chloro-5-hydroxybenzonitrile
https://huagongshe.com/reaction/602586
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | 3-Chloro-5-methoxybenzonitrile | HCID 21949921 | — |
| Solvent | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Product | 3-Chloro-5-hydroxybenzonitrile | HCID 21949878 | 94% |
Reaction Steps
step 2—A 250 mL flask was charged with 5-chloro-3-methoxy-benzonitrile (7.0 g, 41.766 mmol) and 2,4,6-collidine (100 mL). The mixture was heated to 170° C. and LiI (16.76 g, 125.298 mmol) was added and the reaction mixture was heated for 4 h. When R-3b was consumed the reaction was cooled to RT and quenched with 10% aqueous HCl. The resulting mixture was extracted with EtOAc and washed with water and brine. The EtOAc extract was dried over (Na2SO4) and filtered. The solvent was removed in vacuo to afford a yellow oil which was purified by silica gel chromatography eluting with EtOAc/hexane (10:90) to afford 6.0 g (94%) of 3-chloro-5-hydroxy-benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906540B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-7401044e18ca454c806fdd9eb87a851d |
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| Source note | uspto-grants-2011_03 |
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