HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39015Generated: October 26, 2026
Acetone → 2-(Benzyloxy)-1-chloro-3-fluorobenzene
https://huagongshe.com/reaction/39015
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-6-fluorophenol | HCID 2773710 | — |
| Product | 2-(Benzyloxy)-1-chloro-3-fluorobenzene | HCID 53216982 | — |
Reaction Steps
A mixture of 2-chloro-6-fluorophenol (25 g, 170 mmol), acetone (200 ml), K2CO3 (47.08 g, 340 mmol) and bensylbromide (22.31 ml, 187 mmol) was heated at 65° C. for 16 h. The solution was filtered and evaporated. Water (100 ml) was added, and the solution was extracted with EtOAc. The combined organic phases were dried (Na2SO4) and evaporated to dryness to give the title compound (32.3 g). MS m/z (rel. intensity, 70 eV) 236 (M+, 2), 117 (4), 92 (8), 91 (bp), 65 (13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524766B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-38288b2fe72543d2874ba82dd88f7891 |
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| Source note | uspto-grants-2013_09 |
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