HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877955Generated: October 30, 2026
Butylamine → N-butyl-2-((4R,6S)-6-(hydroxymethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetamide
https://huagongshe.com/reaction/877955
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 2-Methylpropan-2-olate | HCID 4574913 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate | HCID 9816650 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-butyl-2-((4R,6S)-6-(hydroxymethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetamide | HCID 53339170 | — |
Reaction Steps
Mixture of tert-butyl 2-((4R,6S)-6-(hydroxymethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate (100 grams), methanol (1 L), n-butyl amine (200 ml) and sodium, tertiary butoxide (74 grams) was heated to 40-45° C. and stirred up to completion of the reaction. Distilled off the reaction mixture completely under reduced pressure and water (300 ml) was added to it at 25-30° C. The reaction mixture was cooled and acidified with aqueous acetic acid. The reaction mixture washed with cyclohexane and product from aqueous layer was extracted into methylene chloride. The organic layer was washed with saturated sodium chloride solution and the solvent from it was distilled off under reduced pressure to get the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987444B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-22dcbc882ac540f9b763ace2352649ca |
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| Source note | uspto-grants-2015_03 |
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