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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955694Generated: October 30, 2026

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

https://huagongshe.com/reaction/1955694

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 (2.5M, 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 numberUS05776959
Source datasetuspto-grants-1998_07
ORD IDord-d9e5479a6ddb42ca8c9810fb47ac4276
Source noteuspto-grants-1998_07