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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425086Generated: October 30, 2026

Diiodomethane → HCID 59557748, compound

https://huagongshe.com/reaction/425086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
Reactant4-Bromo-1-chloro-2-(4-(2-(vinyloxy)ethyl)benzyl)benzeneHCID 59557772—
ReactantHCID 178418750HCID 178418750—
SolventDiethyl EtherHCID 3283—
ProductHCID 59557748HCID 59557748—

Reaction Steps

To a stirred mixture of 4-bromo-1-chloro-2-(4-(2-(vinyloxy)ethyl)benzyl)benzene (100 mg, 0.27 mmol) and Et2Zn (0.68 mL, 0.68 mmol, 1.0 M in hexane) in dry ethyl ether (2 mL) was added diiodomethane (0.06 mL, 0.68 mmol) dropwise during 20 min at room temperature under argon. After stirring overnight, the reaction mixture was poured slowly into ice cold dilute hydrochloride solution with stirring. The mixture was extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with water (10 mL) and then with brine (10 mL), and then dried over sodium sulfate. The residue was concentrated and purified by preparative TLC (eluent EA:PE=1:25) to obtain intermediate CR (86 mg) as a light yellow oil. 1H-NMR (CDCl3, 400 MHz): δ 7.32˜7.24 (m, 3H), 7.18 (d, 2H), 7.12 (d, 2H), 4.05 (s, 2H), 3.73 (t, J=7.2 Hz, 2H), 3.32˜3.29 (m, 1H), 2.88 (t, J=7.2 Hz, 2H), 0.57˜0.44 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106021B2
Source datasetuspto-grants-2012_01
ORD IDord-1aefd59d2e2a4bd4b9abf51b63e8d57e
Source noteuspto-grants-2012_01