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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234327Generated: October 26, 2026

Methyl iodide → 2-Methylbenzo(b)thiophene

https://huagongshe.com/reaction/234327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
Product2-Methylbenzo(b)thiopheneHCID 70952—

Reaction Conditions

Temperature-30 °C

Reaction Steps

t-BuLi (1.7M, 26 mmoles, 15 ml) was added to a stirred solution of benzo[b]thiophene (17 mmoles, 2.3 g) and THF (30 ml) at -50° C. The resulting bright yellow reaction mixture was warmed to -30° C., and iodomethane (26 mmoles, 1.6 ml) was added. After 10 min. at -30° C., the solution was warmed to ambient temperature and stirred an additional 30 min., then diluted with ether (100 ml) and washed with brine (2×100 ml). The organic phase was dried (MgSO4), filtered and concentrated to collect 2.48 g (98%) of 2-methylbenzo[b]thiophene as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594021
Source datasetuspto-grants-1997_01
ORD IDord-7907f0755a9a46be993b5afb3b109fd1
Source noteuspto-grants-1997_01