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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108370Generated: October 31, 2026

Allyl bromide → Methyl 2-ethyl-2-(1-methylethyl)-4-pentenoate

https://huagongshe.com/reaction/1108370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHexamethylphosphoramideHCID 12679—
ReactantLithium diisopropylamideHCID 2724682—
ReactantMethyl 2-ethyl-3-methylbutyrateHCID 12696465—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-ethyl-2-(1-methylethyl)-4-pentenoateHCID 1060755982%

Reaction Steps

The reaction of methyl 2-ethyl-3-methylbutyrate (23.76 g, 165 mmol), prepared as in Lion C, Dubois J E (1981) supra., with allyl bromide (31.34 g, 259 mmol) in the presence of lithium diisopropylamide (prepared by treating diisopropylamine (25.05 g, 248 mmol) with butyllithium in hexanes (2.5 M, 94.4 mL, 236 mmol)) in THF (330 mL) and HMPA (24.7 mL, 142 mmol), as described above in the preparation of Example 7, followed by the vacuum distillation of crude product afforded the pure olefinic ester (24.85 g, 82%) as a colorless liquid: bp 92-94° C. (20 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066666
Source datasetuspto-grants-2000_05
ORD IDord-2eacac5ad4454b9ba4977bd957c5d517
Source noteuspto-grants-2000_05