HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390090Generated: October 29, 2026
Potassium Hydroxide → (SR)-2-((RS)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(methylthio)propan-1-amine
https://huagongshe.com/reaction/390090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 86651336 | HCID 86651336 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ammonia methanol | HCID 21705897 | 7% |
| Product | (SR)-2-((RS)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(methylthio)propan-1-amine | HCID 66953476 | 166% |
Reaction Steps
A solution of benzyl (SR)-2-((RS)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(methylthio)propylcarbamate (50 mg, 147 μmol) and potassium hydroxide (248 mg, 4419 μmol) in isopropanol (2 mL) was heated under reflux for 2 h. Silica gel was added and the mixture was concentrated to dryness, then applied to a silica gel column and eluted with 5% MeOH/CH2Cl2, then 7% 7N NH3/MeOH in CH2Cl2 to give (SR)-2-((RS)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(methylthio)propan-1-amine (25 mg, 122 μmol, 83% yield) as a syrup. 1H NMR (CDCl3) δ 4.20 (1H, dd, J=6.6, 13.5 Hz), 4.06 (1H, dd, J=6.3, 8.0 Hz); 3.70 (1H, t, J=7.7 Hz); 2.82-2.74 (3H, m); 2.61 (1H, dd, J=8.0, 13.0 Hz); 2.13 (3H, s); 1.85-1.75 (1H, m); 1.41 (3H, s); 1.35 (3H, s). 13C NMR (CDCl3) δ 109.1, 76.9, 67.9, 44.5, 42.3, 33.7, 26.9, 25.7, 16.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383636B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-fed532626822435ab672a651a0cf3b84 |
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| Source note | uspto-grants-2013_02 |
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