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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652156Generated: October 29, 2026

Benzoyl chloride, 3,4-dichloro- → HCID 14032554, compound

https://huagongshe.com/reaction/652156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantHCID 178480237HCID 178480237—
SolventDiethyl EtherHCID 3283—
ProductHCID 14032554HCID 1403255457%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole and 8 ml of 3,4-dichlorobenzoyl chloride was heated at 100° C. in a steam bath for 4 hrs. After the reaction mixture cooled to ambient temperature, ether was added and the salt was collected. The salt was mixed with water and ammonium hydroxide solution was added until the mixture was basic. The mixture was warmed on the steam bath for about 5 mins, cooled and extracted with dichloromethane. Evaporation of the dichloromethane in vacuo provided the free base. The base was recrystallized from methanol-trichloromethane (with concentration of the mother liquor) to yield 3.0 g (57%) of product, mp 187°-189° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670447
Source datasetuspto-grants-1987_06
ORD IDord-10100bf4aea94e9da2a2465f70e9b12c
Source noteuspto-grants-1987_06