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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783603Generated: November 2, 2026

Sodium Carbonate → N-(tert-Butoxycarbonyl)-3-(dimethylamino)alanine

https://huagongshe.com/reaction/1783603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant3-(Dimethylamino)alanine--hydrogen chloride (1/2)HCID 44134553—
SolventAcetonitrileHCID 6342—
ProductN-(tert-Butoxycarbonyl)-3-(dimethylamino)alanineHCID 1385098131%
ProductHCID 64796328HCID 64796328—

Reaction Steps

3-Dimethylamino-2-methylamino-propan-1-ol is prepared from 4-aza-DL-leucine 2 HCl. Di-tert-butyl dicarbonate (0.65 g, 2.97 mmol) is added to a biphasic mixture of 4-aza-DL-leucine 2 HCl (0.51 g, 2.47 mmol) in 10 ml 1:1 10% Na2CO3:MeCN. After stirring 16 hours, the MeCN is removed under reduced pressure and the aqueous layer is extracted with ethyl acetate. The aqueous layer is concentrated and purified by reverse phase column chromatography on a sep-pak C18 column (water) yielding 0.19 g (31%) 2-tert-butoxycarbonylamino-3-dimethylamino-propionic acid, sodium salt. The sodium salt is suspended in THF (5 ml) and cooled to 0° C. under N2. LAH (3.8 ml of a 1.0 M solution in THF) is added and the reaction mixture warmed to rt and than to reflux. After stirring at reflux for 16 h, the reaction mixture is cooled to 0° C. and carefully quenched by the slow addition of Na2SO4.10 H2O. The reaction mixture is diluted with diethyl ether, warmed to room temperature and stirred for 30 min. The gray suspension is filtered through Celite and the filtrate concentrated to give 83 mg (82%) of 3-dimethylamino-2-methylamino-propan-1ol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501427B2
Source datasetuspto-grants-2009_03
ORD IDord-87d9d2d9ebbd4c55aa6b5c61a5d99f8c
Source noteuspto-grants-2009_03