HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178449153, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178449157 | HCID 178449157 | — |
| Product | HCID 178449153 | HCID 178449153 | 90% |
Reaction Steps
To an ice-cooled suspension of 1.0 g of N2 -(2-naphthylsulfonyl)-L-arginyl-N-butylglycine in 15 ml of ethanol was added dropwise 0.5 ml of thionyl chloride with vigorous stirring. The reaction mixture was allowed to stand for 2 hours at room temperature and then refluxed for 2 hours. At the end of this period, the reaction mixture was evaporated to dryness, and the residual syrup was treated with cold ethyl ether to give 1.02 g (90%) of N2 -(2-naphthyl-sulfonyl)-L-arginyl-N-butylglycine ethyl ester hydrochloride in the form of a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073891 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-9d504e19b3fd4ca28f2ea3c57290cbb2 |
| Source note | uspto-grants-1978_02 |