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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20825Generated: October 25, 2026

Sodium borohydride → [2-Amino-1-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-1-methyl-2-phenylethyl]dimethylamine

https://huagongshe.com/reaction/20825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant{1-[Amino(phenyl)methyl]cyclopentyl}dimethylamineHCID 11521393—
Reactant2-(Dimethylamino)-3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-2-methylpropanenitrileHCID 86624947—
ReactantHCID 178506676HCID 178506676—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventButyl etherHCID 8909—
Product[2-Amino-1-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)-1-methyl-2-phenylethyl]dimethylamineHCID 6856213233%

Reaction Steps

The title compound (930 mg, 33%) was prepared from 2-(dimethylamino)-3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-2-methylpropanenitrile D47 (2.1 g, 8.67 mmol), phenyl lithium (10.0 ml of a 1.8M solution in dibutyl ether, 18.0 mmol) in THF (30 ml) followed by sodium borohydride (830 mg, 26.0 mmol) in methanol (50 ml) in a similar manner to that described in D2. Chromatography (Biotage Horizon) to isolate the title compound was carried out using (i) 0 to 100% ethyl acetate/pentane, (ii) 100% ethyl acetate and (iii) 0 to 20% methanol/ethyl acetate. The product containing fractions were combined and evaporated. Mass spectrum (Electrospray LC/MS), API+: Found 323 (MH+), 306 (M−16). C18H34N2OSi requires 322. Ret. time 2.35-2.39 min. (broad peak).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745642B2
Source datasetuspto-grants-2010_06
ORD IDord-ab8fe43283da461ba326272650a1c314
Source noteuspto-grants-2010_06