HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389375Generated: October 30, 2026
Hydrochloric Acid → [2-(3-Methoxybenzyl)cyclohexyl]methyl acetate
https://huagongshe.com/reaction/2389375
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | [2-(3-Methoxybenzyl)cyclohexyl]methanol | HCID 68533760 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | [2-(3-Methoxybenzyl)cyclohexyl]methyl acetate | HCID 68535645 | — |
Reaction Steps
To a solution of [2-(3-methoxybenzyl)cyclohexyl]methanol (1.5 g) in pyridine (7.5 mL) was added acetic anhydride (4.1 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 hour and at ambient temperature for 1 hour. The reaction mixture was added 1M HCl aqueous solution and was extracted with EtOAc. The organic layer was washed with 1M HCl aqueous solution and saturated NaHCO3 aqueous solution, and brine. The organic layer was dried over anhydrous MgSO4, filtered and evaporated in vacuo to afford [2-(3-methoxybenzyl)cyclohexyl]methyl acetate (1.57 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273745B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-608214701e9c4c059c81125ff1a97335 |
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| Source note | uspto-grants-2012_09 |
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