HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503424Generated: October 25, 2026
Lithium diisopropylamide → 1-(Pyridazin-3-yl)ethan-1-ol
https://huagongshe.com/reaction/1503424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 6'-Bromospiro[cyclohexane-1,2'-indene]-1',4(3'H)-dione | HCID 58197205 | — |
| Reactant | N-methoxy-N-methylpyridazine-3-carboxamide | HCID 58197546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Pyridazin-3-yl)ethan-1-ol | HCID 15197511 | 106.6% |
Reaction Steps
To a solution of LDA (23.4 mL, 42.1 mmol, 1.8 M in THF) in THF (150 mL) was added slowly a solution of compound 1 (3.6 g, 21.05 mmol) in THF (77 mL) at −60° C. under a N2 atmosphere. After being stirred at −60° C. for 1 h, a solution of compound 2 (7.05 g, 18.9 mmol)) in THF (23 mL) was added slowly to the above solution. The resulting mixture was stirred at −60° C. for 2 h. The reaction mixture was quenched with water (15 mL). The aqueous layer was extracted with EtOAc (3×40 mL). The combined organic layers were washed with brine (20 mL), dried over Na2SO4 and concentrated under reduced pressure to dryness. The residue was purified by column chromatography on silica gel (petroleum:ethyl acetate, 10:1) to give compound 3 (2.5 g, yield 26%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09212153B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-7734bd19058340a4acf9a5ea71277674 |
|---|
| Source note | uspto-grants-2015_12 |
|---|