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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385764Generated: November 1, 2026

Benzyl Bromide → HCID 70048597, compound

https://huagongshe.com/reaction/1385764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium ChlorideHCID 433294—
ReactantLithium diisopropylamideHCID 2724682—
Reactantβ-Hydromuconic acid diethyl esterHCID 6148048—
ProductHCID 70048597HCID 7004859771%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution 688 mg (3.44 mmol) trans-2-butene-1,4-dicarboxylic acid diethyl ester in 35 ml THF was added 1.46 g (34.4 mmol) anhydrous lithium chloride and the resulting suspension cooled to −78° C. 3.44 ml (6.88 mmol) of a 2 M solution of LDA in THF was added dropwise and stirring continued for 45 min. 0.82 ml (6.9 mmol) benzyl bromide was then added and stirring continued for 1 h at −78° C. and 10 min at 0° C. The reaction was quenched at this temperature by addition of saturated ammonium chloride solution and the mixture extracted three times with ether. The combined organic phases were washed with saturated brine, dried over sodium sulphate, and concentrated in vacuo. Flash chromatography (5% EtOAc in hexane) afforded 927 mg (71%) of the title compound as a yellow oil. MS m/e (%): 398 ([M+NH4]+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262089B1
Source datasetuspto-grants-2001_07
ORD IDord-83229691c63048b1958bbbf1fbb0e27b
Source noteuspto-grants-2001_07