HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-t-Butylphenoxy)thioacetamide → HCID 10134842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-t-Butylphenoxy)thioacetamide | HCID 2743912 | — |
| Reactant | 2-Bromo-5-chloro-2,3-dihydro-1H-inden-1-one | HCID 11334069 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10134842 | HCID 10134842 | — |
Reaction Steps
At room temperature, 0.49 g of 2-bromo-5-chlorindan-1-on and 0.45 g of 2-(4-tert-butylphenoxy)-thioacetamide were dissolved in 10 ml of dry acetone, and the mixture was stirred at room temperature for 12 h. The precipitated hydrobromide was filtered off with suction and washed with acetone. The residue was suspended in a little ethyl acetate and treated with saturated sodium bicarbonate solution. The organic phase was separated off, dried over magnesium sulfate, filtered and concentrated under reduced pressure. This synthesis yielded 2-(4-tert-butylphenoxymethyl)-6-chloro-8,8a-dihydroindeno [1,2-d]thiazol-3a-ol having a melting point of 122-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06387935B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-89ecc1b48e754288b7f206b9123014bb |
| Source note | uspto-grants-2002_05 |