HuagongsheHuagongshe Chemistry Print Report · For research reference only
77528-46-2 → 4,5,6,7-Tetrahydro-4-benzothiazolemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 77528-46-2 | HCID 12917739 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,5,6,7-Tetrahydro-4-benzothiazolemethanol | HCID 12917751 | 70% |
Reaction Steps
To a solution of 1.14 g (30 mmoles) of AlLiH4 in 50 ml anhydrous tetrahydrofuran, cooled to -20° C. and maintained at that temperature, are slowly added 6.66 g (30 mmoles) of the above derivative (III) dissolved in 30 ml anhydrous THF. After 30 minutes at -20° C., excess AlLiH4 is destroyed by addition of isopropanol at -20° C. followed by 5 ml saturated aqueous sodium chloride, and is then stirred for 2 hrs. The resulting precipitate is filtered off and washed with ethyl acetate; the filtrate is evaporated and the oily residue is taken up in the hot with hexane; product (IV) crystallizes on cooling. Yield: 70%. M.p.=74°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04423056 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-16e3e0af5995464d8d26565cf0f4f3b7 |
| Source note | uspto-grants-1983_12 |