HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 15885282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Ethyl 5-[[2-(phenylsulfonyl)ethyl]thio]-4-thiazolecarboxylate | HCID 15885293 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15885282 | HCID 15885282 | 650% |
Reaction Steps
To a solution of 4-ethoxycarbonyl-5-[2-(phenylsulfonyl)ethylthio]thiazole (702 mg, 2 mmol) in 20 ml of THF was added lithium borohydride (2M, 1 ml) and methanol (0.16 ml, 4 mmol) at -30° C. The reaction mixture was allowed slowly warm up to room temperature and stirred overnight. The solvent was removed under reduced pressure and the crude residue was subjected to chromatography by using dichloromethane and methanol as the eluent to give the title compound (400 mg, 650%). 1H NMR (CDCl3) δ2.55 (s, 1H), 3.00 (t, 2H, J=6), 3.40 (t, 2H, J=6), 4.71 (s, 2H), 7.6 (t, 2H, J=7), 7.68 (t, 1H, J=7), 7.82 (d, 2H, J=7), and 8.80 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06030965 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-2b6077e4efeb4acd832ec9b0e7577d56 |
| Source note | uspto-grants-2000_02 |