Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68991603 | HCID 68991603 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 86615526 | HCID 86615526 | 46.4% |
Reaction Steps
A mixture of 2.0 grams (5.9 mmol, leq) of 2,9-dichloropentacene-5,7,12,14-tetrone and 3.0 g (322 mmol, 54 eq) of sodium borohydride in 46 mL of 2-methoxyethylether was stirred at 23° C. in a nitrogen atmosphere for 14 hours. To this reaction mixture was added 23 mL of methanol in a dropwise fashion to keep the reaction temperature below 50° C. A solution of 18 grams (96 mmol, 16 eq) of stannous chloride in 19.7 grams of water and 7.3 grams of 12M hydrochloric acid was added at such a rate as to keep the reaction temperature between 23° C. and 40° C. The mixture was stirred for an additional 30 minutes. The reaction mixture was filtered and the residue washed with 46 mL of 12M hydrochloric acid followed by 120 mL of acetone and 40 mL of THF. The solid was dried in air to give 0.95 grams of the desired product. IR KBr 1618 cm−1, 906 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608679B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-5f1821179a7340ccb78047545a1ae34c |
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| Source note | uspto-grants-2009_10 |
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