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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777Generated: October 29, 2026

Thionyl Chloride → HCID 13927511, compound

https://huagongshe.com/reaction/1777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Chloro-4-methoxycarbonyl valeric acidHCID 86752220—
SolventTolueneHCID 1140—
ProductHCID 13927511HCID 13927511—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 7.6 g of 2-chloro-4-methoxycarbonyl valeric acid, 9.2 ml of thionyl chloride and 30 ml of toluene was stirred for 30 minutes at 80° C., followed by distilling off the solvent under reduced pressure to leave 2-chloro-4-methoxycarbonyl butyryl chloride. A mixture of this compound, 5.0 g of 2-benzylaminobenzophenone, 100 ml of ethyl acetate and 100 ml of a saturated aqueous solution of sodium hydrogencarbonate was stirred for 30 minutes at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=5:1) to give 1.2 g of 2-[N-benzyl-N-(2-chloro-4-methoxycarbonyl)butyryl]aminobenzophenone as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726306
Source datasetuspto-grants-1998_03
ORD IDord-9645ae5ef13440c58b9e8e3877a34a9d
Source noteuspto-grants-1998_03