HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453892Generated: October 26, 2026
tert-butyl N-methyl-N-(3-oxopropyl)carbamate → HCID 68490529, compound
https://huagongshe.com/reaction/453892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl N-methyl-N-(3-oxopropyl)carbamate | HCID 10442454 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Reactant | HCID 67369868 | HCID 67369868 | — |
| Reactant | CID 101953985 | HCID 101953985 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68490529 | HCID 68490529 | 84.1% |
Reaction Steps
6.4 g (1.3 eq.) tert-butyl methyl(3-oxopropyl)carbamate were added to a solution of 7.5 g (1 eq.) N,N-dimethyl-4-(thiophen-2-yl)piperidin-4-amine bis hydrochloride in 75 ml methanol at 0° C. and the reaction mixture was stirred for 15 min at 0° C. 4.9 g (3 eq.) sodium cyanoboron hydride were then added in portions and the mixture was stirred for 90 min at room temperature. The reaction course was monitored by thin-layer chromatography (20% MeOH/CHCl3). As the conversion was not yet complete, the pH of the reaction mixture was adjusted to 5-6 with acetic acid and the mixture was stirred for 12 h at room temperature. Once the conversion was complete, the methanol was distilled off, water was added, the mixture obtained was extracted with IPA/chloroform (2×100 ml) and the combined organic phases were dried over Na2SO4. Following removal of the solvent under reduced pressure, the residue was purified by column chromatography (silica gel; 5% MeOH/CHCl3). 8.5 g (84%) of product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492559B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-85641e1ec36a467394266724a740b276 |
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| Source note | uspto-grants-2013_07 |
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