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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627508Generated: October 30, 2026

Methanol → HCID 86662636, compound

https://huagongshe.com/reaction/1627508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Chloro-8-methylquinoline-3-carboxaldehydeHCID 689082—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
CatalystTitanium isopropoxideHCID 11026—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86662636HCID 8666263660.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Chloro-8-methylquinoline-3-carboxaldehyde (5 g, 24.6 mmol) in dry THF (75 mL) was treated with titanium(IV) isopropoxide (14.5 mL, 48 mmol). After 5 minutes, (R)-(−)-2-methyl-2-propanesulfinamide (2.95 g, 24 mmol) was added in one portion and the mixture was stirred for 60 h. The mixture was cooled to 0° C. in a water/ice bath and NaBH4 (1.9 g, 48 mmol) was added. The mixture was stirred for 3 h and cooled to 10° C. MeOH (20 mL) was added dropwise, followed by water (5 mL). The resulting slurry was filtered through Celite and washed thoroughly with EtOAc. The organic layer was washed with water and brine, dried (MgSO4) and the solvent removed in vacuo. The residue was dissolved in MeOH (20 mL) and HCl (4M in 1,4-dioxane; 30 mL). The mixture was stirred for 2 h and, after removing the solvent in vacuo, the residue was dissolved in DCM. The organic layer was washed with sat. NaHCO3 solution, water and brine, then dried (MgSO4), filtered and the solvent removed in vacuo. The residue was redissolved in MeOH and passed through an SCX cartridge, eluting with 0-0.1M MeOH/NH3 in MeOH. The solvent was removed in vacuo and the residue purified by column chromatography on silica, eluting with 0-5% MeOH in EtOAc, to afford the title compound (3 g, 60%). δH (DMSO-d6) 8.50 (1H, s), 7.89 (1H, d, J=8.1 Hz), 7.67 (1H, d, J=7.0 Hz), 7.57 (1H, t, J=7.6 Hz), 4.00 (2H, s), 2.70 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785628B2
Source datasetuspto-grants-2014_07
ORD IDord-220368bce79c49249efed03b09590958
Source noteuspto-grants-2014_07