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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732273Generated: October 29, 2026

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

https://huagongshe.com/reaction/732273

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 2HCl. Di-tert-butyl dicarbonate (0.65 g, 2.97 mmol) is added to a biphasic mixture of 4-aza-DL-leucine 2HCl (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 Na2SO4.10H2O. 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-1-ol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585975B2
Source datasetuspto-grants-2009_09
ORD IDord-be558c6305c347aaa5e753ceee701b03
Source noteuspto-grants-2009_09