HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103788Generated: October 26, 2026
Benzyl Salicylate → Benzyl 2-[2,6-Bis(isopropyl)phenoxycarbonyloxy]-benzoate
https://huagongshe.com/reaction/2103788
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Salicylate | HCID 8363 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Di(propan-2-yl)phenyl carbonochloridate | HCID 271619 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 2-[2,6-Bis(isopropyl)phenoxycarbonyloxy]-benzoate | HCID 21110017 | 57% |
Reaction Steps
To a cooled (0° C.) solution of benzyl salicylate (0.77 g, 3.3 mmol) in dichloromethane (6 mL) was added triethylamine (0.52 mL, 3.7 mmol) and a catalytic amount of DMAP. To this mixture a suspension of compound (104) (0.9 g, 3.7 mmol, crude product from last step) in dichloromethane (4 mL) was further added. The reaction was allowed to warm to room temperature slowly and stirred for 14 h. The reaction mixture was then diluted with 10% aqueous citric acid solution (10 mL) and extracted with ethyl ether (2×40 mL). The organic phase was dried over MgSO4 and concentrated in vacuo. The residue was purified by radial chromatography on silica gel (eluting with ethyl acetate/hexane) to afford 0.8 g (57% yield over two steps) of the title compound (105).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576127B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-274f4251ac5f470e866c915c104f7fc3 |
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| Source note | uspto-grants-2009_08 |
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