HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292977Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 86599000, compound
https://huagongshe.com/reaction/1292977
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | HCID 69420884 | HCID 69420884 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86599000 | HCID 86599000 | — |
Reaction Steps
Analogously to Example 1, 160 mg of 2-cyclohexylmethyl-4-methyl-4-phenyl-1,2-pentanediol is reacted with 342 mg of pyridine-sulfur trioxide complex, 1.95 ml of DMSO and 0.39 ml of triethylamine to form 2-cyclohexylmethyl-2-hydroxy-4-methyl-4-phenylpentanal ('H-NMR (CDCl3); δ=0.90-1.60 (m, 10H), 1.30 (s, 3H), 1.41 (s, 3H), 1.76 (m, 2H), 1.95 (m, 1H), 2.20 (d, 1H), 2.35 (d, 1H), 2.97 (s, 1H), 7.20 (m, 1H), 7.30 (m, 4H), 8.76 (s, 1H)). The crude product is reacted with 137 mg of 5-aminoquinoline and 524 mg of sodium triacetoxy borohydride to form imine (180 mg; 'H-NMR (CDCl3); δ=0.90-1.90 (m, 18H), 2.25 (m, 1H), 2.80 (d, 1H), 3.00 (d, 1 H), 3.76 (t, 1H), 5.06 (d, 1H), 6.25 (d, 1H), 7.10-7.55 (m, 8H), 8.25 (d, 1H), 8.87 (dd, 1H); MS (ESI), 415). Reductive amination with 49 mg of sodium borohydride yields 130 mg of end product after column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238707B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-8decf5d0586641aaa0e2d25efc9755f6 |
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| Source note | uspto-grants-2007_07 |
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