Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031141Generated: October 31, 2026

Ammonium Chloride → HCID 19819833, compound

https://huagongshe.com/reaction/1031141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Methyl-2-thiophenecarboxaldehydeHCID 79911—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 178418336HCID 178418336—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19819833HCID 19819833—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 50 g (0.40 mol) of 3-methyl-2-thiophenecarboxaldehyde in 150 ml of dry tetrahydrofuran at 0° C. was added dropwise 476 ml (0.47 mol) of a 1M solution of lithium bis(trimethylsilyl)amide in tetrahydrofuran over a 2 hour period. After stirring the mixture an additional 20 minutes at 0° C., 476 ml (0.47 mol) of a 1M solution of benzyl magnesium chloride in diethyl ether was added dropwise over a 2 hour period. The resulting mixture was allowed to warm to ambient temperature, stirred for 0.5 h longer, and poured into 2.5 L of saturated aqueous ammonium chloride. The mixture was extracted with chloroform (3×500 ml), organic layers combined, dried over MgSO4, and concentrated to dryness giving 85 g of the title amine as an oil. A sample of the product (4 g) was dissolved in isopropanol, made acidic with hydrogen chloride in isopropanol, decolorized with carbon, and reconcentrated to near dryness. The crude hydrochloride salt was recrystallized from a solvent mixture of ethyl acetate and methanol to give 2.5 g of white solid (mp 184°-186° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05109017
Source datasetuspto-grants-1992_04
ORD IDord-1dd76c4f9667436da9fe946a0dd24ae8
Source noteuspto-grants-1992_04