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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009243Generated: October 30, 2026

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

https://huagongshe.com/reaction/1009243

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 numberUS07973037B2
Source datasetuspto-grants-2011_07
ORD IDord-5c7bcc26877e4cf284bfc3b0b68dae34
Source noteuspto-grants-2011_07