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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722631Generated: November 1, 2026

Oxalyl chloride → HCID 14151761, compound

https://huagongshe.com/reaction/1722631

Reaction equation

Participants

RoleNameHCIDCharge
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 chloride (8 ml) at 5° C. The mixture was stirred for 2 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 numberUS04857513
Source datasetuspto-grants-1989_08
ORD IDord-5c4012131973463b9706dc0719cefe06
Source noteuspto-grants-1989_08