HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477702Generated: November 1, 2026
3,3-Dimethylbutanal → HCID 117839512, compound
https://huagongshe.com/reaction/1477702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3-Dimethylbutanal | HCID 76335 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Reactant | HCID 117839396 | HCID 117839396 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 117839512 | HCID 117839512 | 28.2% |
Reaction Steps
To a dichloromethane solution (1 mL) of 1-(4-chlorobenzyl)-4-(piperazin-1-yl)-1,3,5-triazin-2(1H)-one (31 mg, 0.10 mmol) synthesized in Reference Synthesis Example 9 and 3,3-dimethylbutanal (13 μL, 0.10 mmol), sodium triacetoxyborohydride (42 mg, 0.20 mmol) was added and the resultant mixture was stirred at room temperature for 4 hours. After the completion of the reaction, saturated sodium bicarbonate water was added to the reaction solution and extraction with ethyl acetate from the resultant reaction solution was performed. The organic layer was concentrated under reduced pressure and to the resultant residue, ethyl acetate was added. A resultant solid was filtered and was dried under reduced pressure to obtain the title compound (11 mg, yield: 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403798B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-e70bea16713e410b8e8df449ea2780f4 |
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| Source note | uspto-grants-2016_08 |
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