HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417136Generated: October 30, 2026
Hydrochloric Acid → HCID 178436646, compound
https://huagongshe.com/reaction/1417136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178514331 | HCID 178514331 | — |
| Product | HCID 178436646 | HCID 178436646 | 1,032.7% |
Reaction Steps
The Example 12 illustrates the preparation of a partially substituted polymeric product with a photoactive compound. Example 7 was substantially repeated in Example 12 with the exception of modifications in procedure as set forth below. A 500 ml three-necked round-bottom flask equipped with a magnetic stirrer, water bath, thermometer, nitrogen inlet and bubbler was charged with a solution of poly-4-hydroxystyrene (13.3 g, 110 mmol based on monomer repeat units) in THF (170 g). Triethylamine (6.8 g) was added dropwise and the reaction mixture was allowed to stir for an additional 3-5 minutes. A solution of 6-chlorosulfonyl-3-diazo-4-oxocoumarin (1.6 g, 5.6 mmol) in THF (124 g) was added dropwise and the reaction was allowed to stir at room temperature. After one hour, HPLC analysis showed no residual starting material. The reaction mixture was cooled in an ice bath and neutralized by dropwise addition of conc. HCl (8 g) while maintaining the reaction temperature around 12° C. The reaction mixture was filtered to remove any insoluble impurities. The filtrate was precipitated, with stirring, into ten times its weight of hexane. The resulting slurry was filtered, dried in a vacuum oven overnight at 60° C.; yield 11.2 g of white solids (77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05876897 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-6ae6142c35f7478cbaff39f8404846e6 |
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| Source note | uspto-grants-1999_03 |
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