Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399241Generated: October 31, 2026

Dichloromethane → HCID 178464051, compound

https://huagongshe.com/reaction/2399241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 19387332HCID 19387332—
SolventMethanolHCID 887—
ProductHCID 178464051HCID 17846405187.1%

Reaction Steps

0.100 g (0.148 mmol) 2-[2-(diethylamino)-ethyl]-5-[[2-(diethylamino)ethyl]amino]-7,10-bis(phenylmethoxy)-anthra[1,9-cd]pyrazol- 6(2H)-one is dissolved in cold, dry dichloromethane (4 ml) and boron trichloride (4 ml, 1M solution in dichloromethane) is added dropwise over 30 minutes under argon. The reaction mixture is maintained at 0°-5° C. for 1 hour and then treated dropwise with cold methanol under argon. The mixture is then maintained at room temperature for 2 hours and then evaporated to dryness in vacuo. The resulting crude hydrochloride salt is dissolved in a minimum volume of methanol and then chromatographed on a column of silica gel (60A) using an eluting solvent of dichloromethane:methanol (80:20 v/v) and then dichloromethane:methanol:triethylamine (80:20:1 v/v). The major red band is collected and evaporated in vacuo to yield 0.060 g of the title compound as an orange-red solid, m.p. 152° C.; λmax (methanol) (E/cm/M) 520 nm (22000).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05447950
Source datasetuspto-grants-1995_09
ORD IDord-026f6283fccb482cadf45ab2fd62f8f3
Source noteuspto-grants-1995_09