Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 4-(2,5-Dichlorophenylthio)-3-nitrobenzonitrile | HCID 59548937 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 43518346 | HCID 43518346 | 84.6% |
Reaction Steps
A solution of compound 27 (11.8 g, 36.36 mmol) in THF (200 mL) was combined with a solution of sodium hydrosulfite (37.98 g, 218.1 6 mmol) in water (50 mL). The combined solution was stirred vigorously overnight at 45° C. The reaction was monitored by TLC (25% EtOAc in hexanes), and was complete after 16 hrs as indicated by absence of the starting material. The reaction was removed from heat and THF was evaporated. Aqueous solution was filtered to yield a white solid. The solid was washed with water and dried in a vacuum oven overnight to yield compound 28 (9.077 g, 97% HPLC purity, 84.6% yield). 1H NMR (500 MHz, DMSO-d6): δ 7.55 (d, J=8 Hz, 1H), 7.48 (d, J=8 Hz, 1H), 7.28 (dd, J1=2 Hz, J2=7 Hz, 1H), 7.19 (d, J=2 Hz, 1H), 6.99 (dd, J1=2 Hz, J2=8 Hz, 1H), 6.50 (d, J=2 Hz, 1H), 6.04 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399456B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-e199d3aba72f462984b64a974c7fa91c |
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| Source note | uspto-grants-2013_03 |
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