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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386113Generated: October 30, 2026

Diethyl Ether → Ethylmethylaminotriisopropylgermane

https://huagongshe.com/reaction/2386113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantN-MethylethylamineHCID 12219—
ReactantGermane, chlorotris(1-methylethyl)-HCID 606958—
ReactantButyllithiumHCID 178418339—
ProductEthylmethylaminotriisopropylgermaneHCID 8737540298%

Reaction Steps

A solution of nBuLi (2M in hexanes, 26.34 mL, 42.14 mmol) was slowly added to an ice-cooled solution of ethylmethylamine (3.98 mL, 46.35 mmol) in ether (100 mL). The resulting white mixture was stirred for 2 hours. Triisopropylchlorogermane (9.16 mL, 42.14 mmol) was added dropwise and the reaction mixture slowly warmed to room temperature. The mixture was stirred overnight, the solvent evaporated under vacuum, and the residue washed with pentane (100 mL). The mixture was filtered through a medium glass frit under nitrogen and the solvent evaporated under vacuum to give 10.7 g, 98% of a colorless liquid. The product was purified by fractional distillation (40° C., 75 mtorr). 1H NMR (C6D6): δ 2.87 (q, 2H, 3J=6.9 Hz, NCH2CH3), 2.62 (s, 3H, NCH3), 1.36 (m, CH(CH3)2), 1.18 (d, 18H, 3J=7.2 Hz, CH(CH3)2), 1.11 (t, 3H, 3J=6.9 Hz, NCH2CH3). 13C NMR (C6D6): δ 48.42, 38.22 (NCH2CH3, NCH3), 20.19 (CH(CH3)2), 16.20, 15.79 (NCH2CH3, CH(CH3)2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268665B2
Source datasetuspto-grants-2012_09
ORD IDord-123b5a3c0b724f4a8b27291397307f60
Source noteuspto-grants-2012_09