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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088601Generated: November 1, 2026

Chloride → HCID 14151761, compound

https://huagongshe.com/reaction/1088601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantOxalyl chlorideHCID 65578—
ReactantBenzo(b)thiophene-2-carboxylic acidHCID 95864—
ReactantBenzo[b]thiophene-2-carbonyl ChlorideHCID 142384—
ReactantTetraethyl aminomethylenediphosphonateHCID 2773808—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 14151761HCID 14151761—

Reaction Steps

To a solution of 2-benzo[b]thiophenecarbonyl chloride prepared from 2-benzo[b]thiophenecarboxylic acid (356 mg) and oxalyl chloride (0.35 ml) in methylene chloride (2 ml) was added dropwise a mixture of tetraethyl (aminomethylene)bis(phosphonate) (606 mg), pyridine (316 mg) and trace amounts of 4-(dimethylamino)pyridine in methylene at 5° C. The mixture was stirred for 2 chloride (8 ml) hours at ambient temperature followed by the addition of ethyl acetate. The mixture was washed with water, 1N hydrochloric acid, saturated aqueous solution of sodium bicarbonate and brine successively. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was treated with diisopropyl ether to give tetraethyl [(2-benzo[b]thiophenecarboxamido)-methylene]bis(phosphonate) (790 mg) as a white powder which was recrystallized from a mixture of ethyl acetate and n-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963536
Source datasetuspto-grants-1990_10
ORD IDord-7f2b4c3127df459da2fe537ce27de6b0
Source noteuspto-grants-1990_10