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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879460Generated: October 31, 2026

Dimethylamine → ((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1879460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactanttoluene-4-sulfonic acid (S)-2-tert-butoxycarbonylamino-4,4-dimethyl-pentyl esterHCID 58280488—
SolventPyridineHCID 1049—
SolventPotassium HydroxideHCID 14797—
Product((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-carbamic acid tert-butyl esterHCID 5828049365.2%

Reaction Steps

Dimethylamine (11.2 g, 249.3 mmol, 30.0 equiv) was added portionwise to a stirred solution of toluene-4-sulfonic acid(S)-2-tert-butoxycarbonylamino-4,4-dimethyl-pentyl ester (3.2 g, 8.31 mmol, 1.0 equiv.) in pyridine (9.6 mL) at 0° C. The reaction mixture was slowly warmed to room temperature and stirred for an additional 20 hours at the same temperature. The reaction mixture was diluted with the addition of an aqueous solution of 10% potassium hydroxide (w/v; 30 mL) and was extracted with dichloromethane (3×150 mL). The collected organic extracts were dried over anhydrous sodium sulfate, concentrated under reduced pressure to obtain a crude mass. This was purified by purified by silica gel column chromatography (100-200 mesh) using a gradient of 2-5% methanol/dichloromethane to give ((S)-1-dimethylaminomethyl-3,3-dimethyl-butyl)-carbamic acid tert-butyl ester (1.4 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314250B2
Source datasetuspto-grants-2012_11
ORD IDord-3b116bd77e954d97ae2d9c88fd99ca7d
Source noteuspto-grants-2012_11