Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166839Generated: October 30, 2026

Methyl iodide → 2-Methylbenzo(b)thiophene

https://huagongshe.com/reaction/1166839

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 (1.7 M, 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 numberUS06613804B2
Source datasetuspto-grants-2003_09
ORD IDord-3582fbb193bf4ef1ad9462e928342e42
Source noteuspto-grants-2003_09