Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727931Generated: November 1, 2026

Iodine → Thiophene, 2-(1-naphthalenyl)-

https://huagongshe.com/reaction/727931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-BromonaphthaleneHCID 7001—
Reactant2-BromothiopheneHCID 13851—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductThiophene, 2-(1-naphthalenyl)-HCID 3014303—

Reaction Steps

2-Bromothiophene(1.45 ml, 0.015 m) in diethyl ether (20 ml) was added slowly to magnesium turnings (0.48 g, 0.02 m) and iodine (trace) in diethyl ether (10 ml). It was stirred for 30 min before being added to 1-bromonaphthalene (2.07 g, 0.01 m) and catalyst in diethyl ether (25 ml). The reaction was worked up the usual way yielding a brown oil (2.49 g). The brown oil was purified by column chromatography. Flash silica (104 g) eluted with petroleum ether (600 ml) and increased to 5% diethyl diethyl ether/petroleum ether separated a clear pale green oil (1.50 g, 71% yield); m/z 210 (M+); (Found: C, 80.26; H, 4.91; S, 15.10. C14H10S requires: C, 80.00; H, 4.76; S, 15.24); H NMR (CDCl3), δ7.17 (dd, J=3.2, 5.6 Hz 1H), δ7.23 (dd, J=<1, 3.2 Hz, 1H), δ7.41 (dd, J=<1, 5.6 Hz, 1H), δ7.45 (d, J=4.8 Hz, 1H), δ7.47 (d, J=4.8 Hz, 1H) δ7.48 (d, J=8 Hz, 1H), δ7.55 (dd, J=<1, 8 Hz, 1H), δ7.83 (d, J=8 Hz, 1H), δ 7.88 (dd J=3.2, 4.8 Hz, 1H), δ8.20 (dd, J=5.6, 4.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045563
Source datasetuspto-grants-1991_09
ORD IDord-95ce50f8413d44569b6a7c8b05b38b40
Source noteuspto-grants-1991_09