HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614692Generated: October 29, 2026
Ammonia → 2-Naphthalenesulfonamide, 6,7-dihydroxy-
https://huagongshe.com/reaction/614692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 19832966 | HCID 19832966 | — |
| Reactant | HCID 88763773 | HCID 88763773 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Naphthalenesulfonamide, 6,7-dihydroxy- | HCID 104675 | — |
Reaction Steps
A solution of 20.0 g. (0.0583 mole) of 2,3-diacetoxy-7-naphthalenesulfonyl chloride in 300 ml. of tetrahydrofuran was treated with 8.7 ml. (0.13 mole) of aqueous 28% ammonia. The solid (9.9 g., infrared spectrum identical with that of 6,7-diacetoxy-2-naphthalenesulfonic acid sodium salt) was removed by filtration and the filtrate evaporated to dryness. The residue was dissolved in 150 ml. of ethyl acetate. The residue from evaporation of the dried (anhydrous sodium sulfate) solution was slurried with four 100-ml. portions of ether and then dissolved in 150 ml. of 3A alcohol. The solution was saturated with hydrogen chloride, allowed to stand overnight, and then concentrated at the water pump to give 9.7 g. of colorless residue. Recrystallization from 50 ml. of water gave 5.1 g. (37%) of pale violet solid, m.p. 218°-228° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04145299 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-7e3b51e808e04896b809887f0be248c2 |
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| Source note | uspto-grants-1979_03 |
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