HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 3555469, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclohexyl(2,4-dihydroxyphenyl)methanone | HCID 3673514 | — |
| Product | HCID 3555469 | HCID 3555469 | — |
Reaction Steps
Acetic anhydride (1.58 ml, 16.7 mmol) was added to a solution of 4-cyclohexylcarbonyl resorcinol (1.47 g, 6.68 mmol) in tetrahydrofuran (15 ml) at room temperature, followed by triethylamine (2.80 ml, 20.0 mmol) and the solution stirred for 4 h. At this time, TLC showed the clean formation of a single product (Rf 0.71) and no starting material (Rf 0.40) (Note 5). The solvent was removed under reduced pressure to give 4-cyclohexylcarbonyl resorcinol diacetate as a light-yellow oil (3.0 g) and used without further purification for the next synthetic step (Note 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468464B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-4cb49b552d114a4f8a963213ba33eb93 |
| Source note | uspto-grants-2008_12 |