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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641626Generated: October 31, 2026

Boron Trichloride → HCID 11624627, compound

https://huagongshe.com/reaction/641626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 68579894HCID 68579894—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
ProductHCID 11624627HCID 11624627158.5%

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of 4-[(4-methoxyphenyl)sulfonyl]-5-methyl-4,5-dihydrothieno[3,2-c]isoquinoline (0.45 g, 1.2 mmol) and tetrabutylammonium iodide (1.33 g, 3.6 mmol) in dry methylene chloride (9 mL) was treated dropwise with a solution of boron trichloride in methylene chloride (1.0 M, 3.6 mL, 3.6 mmol) at −78° C. during ca. 5 min. After a further 5 min., the solution was warmed to 23° C. After 16 h the reaction solution was concentrated in vacuo and the residue was taken up in ethyl acetate (25 mL). The organic phase was washed with saturated aqueous sodium bicarbonate (25 mL) and water (10×25 mL), dried (MgSO4), and concentrated in vacuo to give a dark, oily solid (0.68 g) which was suspended in 20% ethyl acetate-hexane and slurried onto a column of silica gel (10 g). Flash chromatography eluting 20-, and then 30% ethyl acetate-hexane gave the product (0.35 g) as a yellow solid. Recrystallization from hot ethyl acetate-hexane gave the title compound (0.28 g, 65%, m.p. 163-65° C.) as shiny white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696221B2
Source datasetuspto-grants-2010_04
ORD IDord-16dca5d652184281b164d8879e236fd1
Source noteuspto-grants-2010_04