HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174462Generated: October 27, 2026
Diethyl Ether → Ethylmethylaminotriisopropylgermane
https://huagongshe.com/reaction/1174462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | Germane, chlorotris(1-methylethyl)- | HCID 606958 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | Ethylmethylaminotriisopropylgermane | HCID 87375402 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838329B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-e93a398abbf941ebbde924b54f09630c |
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| Source note | uspto-grants-2010_11 |
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