HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78235Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 59255198, compound
https://huagongshe.com/reaction/78235
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Benzylsulfanyl-4-((E)-2-nitro-vinyl)-benzene | HCID 59255337 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59255198 | HCID 59255198 | 97.8% |
Reaction Steps
To a solution of 1-benzylsulfanyl-4-((E)-2-nitro-vinyl)-benzene (950 mg, 3.5 mmol) described in Manufacturing Example 205-1-3 in acetic acid (0.6 mL) and dimethyl sulfoxide (10 mL) was added sodium borohydride (212 mg, 5.6 mmol) while the internal temperature was held at 30° C. or lower, which was stirred for 30 minutes at room temperature. The mixture was cooled with ice water, water was added, which was stirred for another 30 minutes. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (936 mg). The title compound was used in the following reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841327B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-dadb4748695d472cb63b1522be131323 |
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| Source note | uspto-grants-2014_09 |
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