HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropylamine → HCID 13763878, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 9,10-Anthracenedione, 1,4-bis[[(4-methylphenyl)sulfonyl]oxy]- | HCID 384116 | — |
| Product | HCID 13763878 | HCID 13763878 | 76% |
Reaction Steps
1-(isopropylamino)-4-tosyloxyanthraquinone was prepared by reaction of 1,4-ditosyloxyanthraquinone with isopropyl amine. The isolated and purified reaction product has the structure illustrated below (where "Ts" is ##STR8## The yield was 76% and the m.p. 164°-165° C.; mass spec m/e/ 435 (M+), 420 (M-CH3), 280 (M-C7H7SO2), 238 (280-CH3H7 +H), 210 (238-CO), 182 (210-CO), 155 (C7H7SO2), 91 (C7H7); 1H-NMR (CD2Cl2)δ9.97 (br s, 1H), 8.19-8.10 (m, 2H), 7.85-7.67 (m, 4H), 7.27-6.97 (m, 4H), 4.02-3.68 (m, 1H), 2.30 (s, 3H), 1.38, 1.31 (d, 6H); IR (Nujol) 1180 cm-1 (symmetrical SO2 stretch), 890 cm-1, 860, 820, 780 (S--O--C stretch); UV/VIS max (Xylenes(500 nm (ε6660).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04746461 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-7822c0891bbd47f6a7a8fb76522996a9 |
| Source note | uspto-grants-1988_05 |