HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57408Generated: October 27, 2026
Potassium Carbonate → tert-Butyl (2S)-but-3-yn-2-ylcarbamate
https://huagongshe.com/reaction/57408
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-butyl N-((2S)-1-oxopropan-2-yl)carbamate | HCID 7015728 | — |
| Reactant | (1E)-1-diazo-1-dimethoxyphosphorylpropan-2-one | HCID 136023029 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl (2S)-but-3-yn-2-ylcarbamate | HCID 10986677 | 53% |
Reaction Steps
A solution of (S)-tert-butyl(1-oxopropan-2-yl)carbamate (500 mg, 2.89 mmol), dimethyl(1-diazo-2-oxopropyl)phosphonate (610 mg, 3.18 mmol, 1.1 equiv), and potassium carbonate (638 mg, 4.62 mmol, 1.6 equiv) in methanol (14.4 mL) was stirred at room temperature for 18 hours. The reaction was then diluted with ethyl acetate (30 mL) and saturated aqueous sodium chloride (40 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (30 mL) and the combined organic extracts were dried over Na2SO4, filtered and concentrated. Silica gel column chromatography (20% EtOAc in Heptane) provided (S)-tert-butyl but-3-yn-2-ylcarbamate (0.258 g, white solid) in 53% yield. 1H NMR (400 MHz, CDCl3) δ 4.49 (m, 1H), 2.26 (d, J=2.2 Hz, 1H), 1.46 (s, 9H), 1.41 (d, J=6.8 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-3b3c45eaca954158b78654fa10bad086 |
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| Source note | uspto-grants-2016_09 |
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