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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480231Generated: November 1, 2026

Heptane → HCID 90203887, compound

https://huagongshe.com/reaction/1480231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptaneHCID 8900—
Reactant4-MethylthiazoleHCID 12748—
ReactantLithium diisopropylamideHCID 2724682—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 59599164HCID 59599164—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 90203887HCID 9020388769%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 2.0M solution of lithium diisopropylamide in THF (492 μl, 984 μmol) was added dropwise to a solution of 4-methylthiazole (97.5 mg, 984 μmol) in dry THF (0.3 ml) cooled to −78° C. and once the addition was complete the reaction was stirred for 30 minutes at −78° C. followed by addition of dry toluene (0.6 ml). To a solution of 2-methyl-N-(2H-pyran-4(3H,5H,6H)-ylidene)propane-2-sulfinamide (CAN 861857-62-7, 100 mg, 492 μmol) in dry toluene (1 mL) was added a 2.0M solution of trimethylaluminum in heptane (271 μl, 541 μmol). The former solution was then added to the reaction mixture cooled at −78° C. The reaction was allowed to warm up to room temperature overnight. The reaction was quenched by the addition of a saturated aqueous solution of ammonium chloride and was then diluted with ethyl acetate. The bi-phasic mixture was poured into a separatory funnel and extracted. The organic phase was collected, dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a dichloromethane/methanol gradient to yield the title compound (102 mg, 69%). MS (ESI, m/z): 303.5 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-372c2a2a3dd145c2a634773624fbfc3f
Source noteuspto-grants-2016_08