Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86758847 | HCID 86758847 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21225906 | HCID 21225906 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06524764B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-c66f1fcfcaf24cbbba0e4c41e9dfce80 |
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| Source note | uspto-grants-2003_02 |
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