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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962763Generated: October 30, 2026

Hydrochloric Acid → HCID 19085567, compound

https://huagongshe.com/reaction/962763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(Phenylsulfonyl)-1H-indoleHCID 315017—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-Benzyloxy-3-(3-chloropropoxy)benzoic acidHCID 19085564—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 19085567HCID 19085567—
Product3-(3-Chloropropoxy)-4-benzyloxybenzoyl chlorideHCID 19085585—

Reaction Steps

3-(3-Chloropropoxy)-4-benzyloxybenzoyl chloride, which was prepared using 4-benzyloxy-3-(3-chloropropoxy)benzoic acid (2.53 g) and oxalyl chloride (1 ml), was dissolved in dichloroethane (20 ml). Aluminum chloride (2.63 g) was added to the resultant solution while cooling on ice bath, stirred for 5 minutes at room temperature, and then cooled again on ice bath. 1-(Phenylsulfonyl)indole (1.69 g) in dichloroethane (10 ml) was added dropwise to the resultant mixture and stirred for 2.5 hours at room temperature. The reaction mixture was poured into 1N HCl and extracted with ethyl acetate. The resultant extract was sequentially washed with saturated sodium bicarbonate solution and brine and then dried. The solvent was distilled off. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1), obtaining 0.76 g of 3-[4-hydroxy-3-(3-chloropropoxy)benzoyl]-1-(phenylsulfonyl) indole as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760040
Source datasetuspto-grants-1998_06
ORD IDord-e703061c645d43679835b9f1a482828e
Source noteuspto-grants-1998_06