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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620906Generated: October 30, 2026

Dichloromethane → {[(2S)-2-amino-4-methylpentyl]oxy}(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/1620906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantL-LeucinolHCID 111307—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Product{[(2S)-2-amino-4-methylpentyl]oxy}(tert-butyl)dimethylsilaneHCID 11345273—

Reaction Steps

To a room temperature dichloromethane (100 mL) solution of L-leucinol (6.0 g) was added triethylamine (11 mL), DMAP (0.1 g) and t-butyldimethylsilyl chloride (8.5 g). The mixture was stirred at room temperature for 2 hours and then water was added. The organic layer was separated and the aqueous further extracted with dichloromethane. The combined organic layers were washed with brine, dried with magnesium sulfate and the solvent was removed in vacuo to yield the title compound, a residue which was used as such in the next reaction. 1H NMR (CD3COCD3) δ 3.48 (m, 2H), 3.32 (m, 1H), 2.76 (m, 1H), 1.78 (m, 1H), 1.22-1.02 (m, 2H), 0.88 (m, 15H), 0.06 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772336B2
Source datasetuspto-grants-2014_07
ORD IDord-390795ab339042a2aa5ff6572f4b1a6f
Source noteuspto-grants-2014_07