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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977532Generated: October 29, 2026

Iodine → HCID 19705711, compound

https://huagongshe.com/reaction/977532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant6-Methoxy-1-benzothiopheneHCID 13634237—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19705711HCID 1970571175.7%

Reaction Steps

To a solution of 6-methoxybenzo[b]thiophene (5.00 g, 30.49 mmol) in 200 mL of anhydrous THF at -78° C., was added n-butyllithium (20.0 mL, 32.01 mmol, 1.6M solution in hexanes). After stirring for 15 minutes, a solution of I2 (8.10 g, 32.01 mmol) in 25 mL of anhydrous THF was introduced dropwise via canula. The resulting mixture was allowed to gradually warm to ambient temperature. The reaction was quenched by distributing between ethyl acetate/brine (150 mL each). The layers were separated and the organic layer was dried over sodium sulfate. Concentration in vacuo produced a tan solid that was recrystallized from hexanes to provide 6.70 g (75%) of 6-methoxy-2-iodobenzo [b]thiophene. mp 75°-77° C. 1H NMR (CDCl3) d 7.59 (d, J=8.6 Hz, 1H), 7.42 (s, 1H), 7.22 (d, J=2.0 Hz, 1H), 6.92 (dd, J=8.6, 2.0 Hz, 1H) , 3.86 (s, 3H) . FD mass spec: 290. Anal. Calcd. for C9H7OSI: C, 37.26; H, 2.43. Found: C, 37.55; H, 2.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614639
Source datasetuspto-grants-1997_03
ORD IDord-86cc2ea1ddcb46639dc9c4e3302ece8c
Source noteuspto-grants-1997_03