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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060517Generated: November 3, 2026

Bisphenol A → HCID 21225906, compound

https://huagongshe.com/reaction/1060517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBisphenol AHCID 6623—
ReactantTriethylamineHCID 8471—
ReactantHCID 86758847HCID 86758847—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21225906HCID 21225906—

Reaction Conditions

Temperature40 °C

Reaction Steps

11.4 g (0.05 mol) of bisphenol A (result of calculation of dipole moment based on MOPAC-97=2.1 debye) and 34.9 g (0.13 mol) of 5-naphthoquinone diazide sulphonyl chloride were dissolved in 400 g of 1,4-dioxane under a current of dry nitrogen, and then warmed to 40° C. To this there was added, dropwise, 13.1 g (0.13 mol) of triethylamine mixed with 40 g of 1,4-dioxane, and then naphthoquinone diazide compound (4) was obtained in the same way as in Synthesis Example 1. (As an average, 1.3 of the Q groups=5-naphthoquinone diazide sulphonyl groups and 0.7=hydrogen.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06524764B1
Source datasetuspto-grants-2003_02
ORD IDord-c66f1fcfcaf24cbbba0e4c41e9dfce80
Source noteuspto-grants-2003_02