HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579545Generated: October 25, 2026
Tetrahydrofuran → 1,1-Dimethylethyl 2-[(diphenylmethylene)amino]-5-hexenoate
https://huagongshe.com/reaction/579545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | N-(Diphenylmethylene)glycine tert-butyl ester | HCID 688171 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,1-Dimethylethyl 2-[(diphenylmethylene)amino]-5-hexenoate | HCID 16066974 | 94% |
Reaction Steps
While under an atmosphere of argon, a solution of N-(diphenylmethylene)glycine tert-butyl ester (6.30 g, 21.33 mmol) and 4-bromo-butene (3.45 g, 25.56 mmol) in freshly distilled THF (50 mL) was cooled to −78° C. and treated with sodium bis(trimethylsilyl)amide (23.4 mL, 1.0 M in THF). Once the addition was complete, the reaction was warmed to room temperature and stirred for 16 h, cooled to 0° C., diluted with ethyl ether and washed successively with saturated aqueous NaHCO3 and saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. Rapid purification by MPLC (1-25% ethyl acetate in heptane over 8 CV) gave product tert-butyl 2-(diphenylmethyleneamino)hex-5-enoate as a colorless oil (7.00 g, 94%). Rf 0.50 (30% ethyl acetate in heptane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040703B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-3f97ef19311e49cc876029c1e88f0688 |
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| Source note | uspto-grants-2015_05 |
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