HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843958Generated: October 26, 2026
Ethyl Acetate → (5-Fluoro-1-benzothiophen-2-yl)methanol
https://huagongshe.com/reaction/1843958
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Methyl 5-fluoro-1-benzothiophene-2-carboxylate | HCID 22473847 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (5-Fluoro-1-benzothiophen-2-yl)methanol | HCID 36995594 | 83.33% |
Reaction Steps
DIBAL-H (59.4 mL, 59.41 mmol) was added to a solution of methyl 5-fluorobenzo[b]thiophene-2-carboxylate (I-50a: 2.5 g, 11.882 mmol) in THF (75 mL) at −70° C. and the resulting reaction mass was stirred at −10° C. for 2 hours. The reaction was monitored by TLC (30% ethyl acetate in hexane). The reaction mass was quenched with methanol at −70° C. and concentrated under reduced pressure. The crude residue obtained was partitioned between water and ethyl acetate. The organic layer was dried over Na2SO4 and concentrated under reduced pressure to afford the crude product. Purification by column chromatography on silica gel (15% ethyl acetate in hexane) afforded 1.8 g of the product (83.33% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946260B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-5f9944555000483286c8ad2335b14e60 |
|---|
| Source note | uspto-grants-2015_02 |
|---|