HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22484967, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22484955 | HCID 22484955 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22484967 | HCID 22484967 | — |
Reaction Steps
A crude product (1.17 g) of N-tert-butyl-4-hydroxybutane-sulfonamide was dissolved in pyridine (3.0 ml) and acetic anhydride (1.5 ml) was added, and the mixture was left standing at room temperature for 1 hr. The reaction mixture was concentrated to dryness under reduced pressure and the residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed once with water and once with saturated brine, dried over magnesium sulfate and concentrated to dryness under reduced pressure to give N-tert-butyl-4-acetoxybutanesulfonamide (425 mg) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890934B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-36512cf2f46d426e8d26832aeb5028d7 |
| Source note | uspto-grants-2005_05 |