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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038521Generated: October 30, 2026

Diiodomethane → 4-Bromo-1-chloro-2-(4-(cyclopropoxymethyl)benzyl)benzene

https://huagongshe.com/reaction/2038521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantHCID 59557768HCID 59557768—
ReactantHCID 178418750HCID 178418750—
SolventDiethyl EtherHCID 3283—
Product4-Bromo-1-chloro-2-(4-(cyclopropoxymethyl)benzyl)benzeneHCID 59557757—

Reaction Steps

To a stirred mixture of 4-bromo-1-chloro-2-(4-(vinyloxymethyl)benzyl)benzene (0.7 g, 2.07 mmol) and Et2Zn (5.18 mL, 5.18 mmol, 1.0 M in hexane) in dry ethyl ether (10 mL) was added diiodomethane (0.42 mL, 5.18 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 (3×20 mL). The combined organic layers were washed with water (20 mL) and then with brine (20 mL), and then dried over sodium sulfate. The residue was concentrated and purified by column chromatography (eluent EA:PE=1:200) to obtain intermediate CV (0.6 g) as a colorless oil. 1H NMR (CDCl3, 400 MHz): δ 7.33˜7.24 (m, 5H), 7.18 (d, 2H), 4.55 (s, 2H), 4.07 (s, 2H), 3.40˜3.37 (m, 1H), 0.69˜0.49 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575321B2
Source datasetuspto-grants-2013_11
ORD IDord-d16991501e754c86808dcc151aba88c7
Source noteuspto-grants-2013_11