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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304368Generated: November 1, 2026

Succinic anhydride → HCID 86758459, compound

https://huagongshe.com/reaction/2304368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSuccinic anhydrideHCID 7922—
ReactantTriethylamineHCID 8471—
Reactantp-Hydroxyaniline mustardHCID 71000—
SolventChloroformHCID 6212—
ProductHCID 86758459HCID 8675845983%

Reaction Steps

To a suspension of succinic anhydride (225 mg, 2.25 mmol) in CHCl3 (10 ml) was added under stirring, 4-[N,N-bis(2-chloroethyl)-amino]phenol (compound 6, FIG. 7; 203 mg, 0.75 mmol) followed by triethylamine (75 mg, 0.75 mmol). The mixture was stirred overnight and the solvent evaporated. The crude residue was dissolved in EtOAC/Et2O/H2O and under stirring the pH was adjusted to 3. The organic layer was washed with water, brine, dried (MgSO4), and evaporated. The resulting oil was crystallised from Et2O/hexane and the white solid was filtered off and dried under vacuum to obtain the desired end product (210 mg; yield 83%). Melting point 98-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436691B1
Source datasetuspto-grants-2002_08
ORD IDord-a9a030a72b8048f7a5cab87c596b41be
Source noteuspto-grants-2002_08