HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 5-Bezyloxy-3-acetoxymethythio-1,2,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole | HCID 23032447 | — |
| Product | 5-Bezyloxy-3-acetoxymethythio-1,2,4-thiadiazole | HCID 58962894 | 64.5% |
Reaction Steps
Into 1.5 g of acetic anhydride were added 620 mg of 2,6-lutidine and 500 mg of 5-benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole under ice-cooling. After stirring for 15 hours at room temperature, the reaction mixture was added to saturated sodium hydrogen carbonate aqueous solution, and extracted with t-butyl methyl ether. The organic layer was concentrated, and the residue obtained was subjected to silica gel column chromatography to give 376 mg of 5-bezyloxy-3-acetoxymethythio-1,2,4-thiadiazole (hereinafter, referred to as the present compound (44)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07273879B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-54c407c5d82d447f93314033ab40fc69 |
| Source note | uspto-grants-2007_09 |