HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895565Generated: October 25, 2026
6,13-Pentacenequinone → HCID 178521537, compound
https://huagongshe.com/reaction/1895565
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6,13-Pentacenequinone | HCID 76415 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178521537 | HCID 178521537 | 91% |
Reaction Steps
To a suspension of 6,13-pentacenequinone (1.0 g, 3.24 mmol) in dry MeOH (40 mL) at 0° C. under an argon atmosphere was slowly added NaBH4 (1.22 g, 32.46 mmol). The reaction mixture was stirred at 0° C. for 0.5 h and at RT for 1 h, and then quenched with H2O at 0° C. The resulting mixture was filtered and washed with H2O. The resulting solid was taken up in CHCl3, then filtered and washed with CHCl3, and dried in vacuo to give product as an off-white solid (0.92 g, 91%): mp 235° C. 1H NMR (500 MHz, DMSO-d6): δ 8.12 (s, 4H), 7.95 (m, 4H), 7.48 (m, 4H), 6.63 (s, 2H), 5.81 (s, 2H). 13C NMR (125.68 MHz, DMSO-d6): δ 138.19, 131.67, 127.47, 125.44, 120.91, 66.98. LDI-MS m/z: 312 [M+], 296 [M+-OH], 280 [M+-2(OH)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513466B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-be057a0002e1450a959314afc1d4a9d8 |
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| Source note | uspto-grants-2013_08 |
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