HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 22628263, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | 1-(Ethenesulfonyl)piperazine | HCID 22628108 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | HCID 22628263 | HCID 22628263 | — |
Reaction Steps
A solution of 1-(ethenesulfonyl)piperazine (1.38 g), salicylaldehyde (610 mg) and potassium tert-butoxide (168 mg) in tert-butanol (20 ml) was refluxed for 4 days. The reaction solution was concentrated, and to the residue was added ethyl acetate. The organic layer was washed with water and brine, dried, concentrated and purified with silica gel column chromatography (hexane/ethyl acetate=2/1) to give a colorless solid of 1-(2H-benzopyrane-3-sulfonyl)-4-(tert-butoxycarbonyl)piperazine (420 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06359134B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-23e071bc82c84d3ea7a678da1427c7a2 |
| Source note | uspto-grants-2002_03 |