HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641626Generated: October 31, 2026
Boron Trichloride → HCID 11624627, compound
https://huagongshe.com/reaction/641626
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 68579894 | HCID 68579894 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11624627 | HCID 11624627 | 158.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696221B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-16dca5d652184281b164d8879e236fd1 |
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| Source note | uspto-grants-2010_04 |
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