HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607204Generated: October 29, 2026
Acetic Acid → 4-(4-Benzylamino-2-nitro-phenylsulfanyl)-phenol
https://huagongshe.com/reaction/607204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-(4-Amino-2-nitro-phenylsulfanyl)-phenol | HCID 66808437 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-Benzylamino-2-nitro-phenylsulfanyl)-phenol | HCID 66808476 | 77.7% |
Reaction Steps
A solution of the product of Example 84A (0.63 g, 2.4 mmol), benzaldehyde (0.24 g, 2.3 mmol) and sodium cyanoborohydride (0.15 g, 2.4 mmol) in methanol (10 mL) containing 1% acetic acid was stirred at room temperature for 16 hours. The reaction mixture was quenched with water (20 mL) and the resultant solution was concentrated under vacuum to a yellow solid. The solid was dissolved in ethyl acetate (50 mL), and washed with water, 10% sodium bicarbonate and 10% sodium chloride. The organic layer was dried over anhydrous sodium sulfate, filtered and solvent removed under vacuum leaving a light yellow oil. The oil was purified by silica gel chromatography eluting with 1% methanol in methylene chloride to provide the title compound (0.63 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915411B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-f4224b0780894c1eb1bd1972861539a8 |
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| Source note | uspto-grants-2011_03 |
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