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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 86651336HCID 86651336—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductAmmonia methanolHCID 217058977%
Product(SR)-2-((RS)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-(methylthio)propan-1-amineHCID 66953476166%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383636B2
Source datasetuspto-grants-2013_02
ORD IDord-fed532626822435ab672a651a0cf3b84
Source noteuspto-grants-2013_02