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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417136Generated: October 30, 2026

Hydrochloric Acid → HCID 178436646, compound

https://huagongshe.com/reaction/1417136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantHCID 178514331HCID 178514331—
ProductHCID 178436646HCID 1784366461,032.7%

Reaction Conditions

Temperature12 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05876897
Source datasetuspto-grants-1999_03
ORD IDord-6ae6142c35f7478cbaff39f8404846e6
Source noteuspto-grants-1999_03