HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Hydroxysuccinimide → 2,3-Dihydroxy-5-(4-methyl-benzoyl)-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | N-Cyclohexylcarbodiimide | HCID 12048208 | — |
| Reactant | 2,3-Dihydroxy-5-(4-methyl-benzoyl)-benzoic acid | HCID 59643045 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3-Dihydroxy-5-(4-methyl-benzoyl)-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester | HCID 59643004 | — |
Reaction Steps
To a solution of 2,3-dihydroxy-5-(4-methyl-benzoyl)-benzoic acid (214 mg, 0.79 mmol) in 10 mL dry THF cooled to 0° C., N-hydroxysuccinimide (136 mg, 1.18 mmol, 1.5 eq.) and N-cyclohexylcarbodiimide, N′-methyl polystyrene HL (Novabiochem) (1.9 eq./g, 832 mg, 2 eq.) were added and the solution was stirred 14 h while the cooling bath slowly warmed up to r.t. The solution was filtered and the filtrate was evaporated under reduced pressure. The crude product was recrystallised from H2O to yield the desired product as a brownish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07319101B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-21c3dfd2e9dc4f5797e2b82d870b2288 |
| Source note | uspto-grants-2008_01 |