HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 17934659, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | tert-Butyl 4-hydroxybenzoate | HCID 117640 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 17934659 | HCID 17934659 | 87.1% |
Reaction Steps
Trifluoromethanesulfonic anhydride (1.04 ml, 6.2 mmol) was added to a cooled (5° C.) solution of tert-butyl 4-hydroxybenzoate (1 g, 5.1 mmol) in a mixture of DCM (25 ml) and TEA (1.1 ml, 7.8 mmol). After 4 h at 5° C., water was added. The organic layer was separated, dried over MgSO4 and concentrated in vacuo. The residue was chromatographed over silica gel (eluent: cyclohexane/iPr2O 95/5) to yield the above-titled compound as a colorless oil (1.45 g). 1H NMR (CDCl3): 8.09 (2H, d, J=8.6 Hz), 7.32 (2H, d, J=8.6 Hz), 1.60 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06977267B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-ba8d1a6d6ea141dfb286a494f23b81fe |
| Source note | uspto-grants-2005_12 |