HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050767Generated: October 26, 2026
Acetic Acid → Ethyl 3-phenyl-2-(tert.butylaminosulfonyl)prop-2-enoate
https://huagongshe.com/reaction/2050767
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | ethyl-2-(N-tert-butylsulfamoyl)acetate | HCID 19833529 | — |
| Product | Ethyl 3-phenyl-2-(tert.butylaminosulfonyl)prop-2-enoate | HCID 57037021 | 72% |
Reaction Steps
11.2 g (0.05 mol) of ethyl 2-(tert.butylaminosulfonyl)acetate (see J. Org. Chem. 43, p. 4535 (1978)) are dissolved in 50 ml of benzaldehyde, 2 g of ammonium acetate and 2 ml of glacial acetic acid are added, and the mixture is stirred for 2 hours at 60° C. under a water pump vacuum (20 mm). The excess aldehyde is subsequently distilled off, and the residue is digested using n-hexane and recrystallized from isopropanol. 11.2 g (72% of theory) of ethyl 3-phenyl-2-(tert.butylaminosulfonyl)prop-2-enoate of melting point 111°-113° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05015284 |
|---|
| Source dataset | uspto-grants-1991_05 |
|---|
| ORD ID | ord-50e92ea2e822489f80998c8691832cdf |
|---|
| Source note | uspto-grants-1991_05 |
|---|