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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092001Generated: October 28, 2026

Methyl iodide → HCID 178500469, compound

https://huagongshe.com/reaction/2092001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexaneHCID 8058—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 178500717HCID 178500717—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178500469HCID 17850046980%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of trans-(3-benzyloxy-cyclobutyl)-acetic acid methyl ester (110 mg, 0.47 mmol) in THF (1 mL) is added 1.09M LDA in THF and hexane (1.51 mL, 1.65 mmol) at −78° C. under nitrogen, and stirred at −78° C. for 30 min. To the mixture, iodomethane (232 ul, 3.76 mmol) is added, and the mixture is stirred at −78° C. for 30 min. The temperature is slowly warmed to room temperature for 3 hours. To the mixture, H2O is added and extracted with AcOEt. The organic layer is dried over MgSO4 and concentrated under reduced pressure to give trans-2-(3-benzyloxy-cyclobutyl)-propionic acid methyl ester (94 mg, 80%); ESI-MS m/z 249 [M+1]+, retention time 2.07 min (condition A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440682B2
Source datasetuspto-grants-2013_05
ORD IDord-6508e55936ed46f79e3446d010947877
Source noteuspto-grants-2013_05