HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891084Generated: November 1, 2026
Water → Ethyl [(4-aminophenyl)(methyl)oxido-sulfanylidene]carbamate
https://huagongshe.com/reaction/1891084
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (RS)-N-(ethoxycarbonyl)-S-methyl-S-(4-nitrophenyl)sulfoximide | HCID 59674069 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl [(4-aminophenyl)(methyl)oxido-sulfanylidene]carbamate | HCID 44122615 | 100% |
Reaction Steps
A solution of 8.70 g (32.0 mmol) of (RS)—N-(ethoxycarbonyl)-S-methyl-S-(4-nitrophenyl)sulfoximide in 650 ml of THF is slowly mixed at room temperature with 435 ml of a 10% solution of Ti(III)Cl in approximately 10% hydrochloric acid (Aldrich). The batch is stirred for 4 hours at room temperature and then cooled to 0° C. 450 ml of a 32% NaOH solution is added in drops. In this case, the reaction mixture is now diluted by the addition of water and ethyl acetate. It is mixed with 500 ml of ethyl acetate, and the organic phase is separated. The pulpy, aqueous phase is extracted from ethyl acetate. The combined organic phases are washed with dilute NaCl solution, dried (Na2SO4), filtered and concentrated by evaporation. 8.05 g (about 32.0 mmol) of the product is obtained, and said product is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08507510B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-896d8f4a81824f55937d87d0d5620201 |
|---|
| Source note | uspto-grants-2013_08 |
|---|