HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109290Generated: October 30, 2026
Chlorosulfonyl isocyanate → HCID 54381889, compound
https://huagongshe.com/reaction/1109290
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 5-(3,5-Bis(tert-butyl)-4-hydroxyphenyl)methylene-4-thiazolidinone | HCID 130003 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54381889 | HCID 54381889 | 69.3% |
Reaction Steps
5-(3,5-Di-tert-butyl-4-hydroxybenzylidene)thiazolidin-4-one (479 mg, 1.5 mmole) described in Kokai 62-42977 was suspended in dried toluene (3 ml), to which chlorosulfonyl isocyanate (144 μl;1.65 mmole) was added with stirring under nitrogen atmosphere, to obtain a transparent solution of orange color. Furthermore, the solution was heated at 90° C. for 10 min., from which toluene was evaporated under reduced pressure, then 3.6 ml of mixed solution of acetic acid and water (2:1) was added thereto. The resulting mixture was heated at 90° C. for 10 min. and poured into ice-water, which was subjected to extraction with dichloromethane. The obtained organic layer was washed with water and saturated brine, dried over magnesium sulfate, and evaporated. The obtained residue was separated by using silica gel chromatography (chloroform:acetone=20:1), whereby 377 mg of the objective compound was obtained, which was recrystallized from ethanol-ether in 53% yield. The physical constants are described on Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05319100 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-53341ae822a442ccb8fda710e2eb2137 |
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| Source note | uspto-grants-1994_06 |
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