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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425097Generated: October 30, 2026

Diiodomethane → HCID 59557763, compound

https://huagongshe.com/reaction/425097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantHCID 59557752HCID 59557752—
ReactantHCID 178418750HCID 178418750—
SolventDiethyl EtherHCID 3283—
ProductHCID 59557763HCID 59557763—

Reaction Steps

To a stirred mixture of 4-bromo-1-chloro-2-(4-(3-(vinyloxy)propyl)benzyl)benzene (0.75 g, 2.04 mmol) and Et2Zn (5.11 mL, 5.11 mmol, 1.0 M in hexane) in dry ethyl ether (10 mL) was added diiodomethane (0.41 mL, 5.11 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 preparative TLC (eluent EA:PE=1:40) to obtain intermediate DH (0.64 g) as a light yellow oil. 1H NMR (CDCl3, 400 MHz): δ 7.32˜7.25 (m, 3H), 7.15 (d, 2H), 7.11 (d, 2H), 4.05 (s, 2H), 3.53 (t, J=6.4 Hz, 2H), 3.31˜3.26 (m, 1H), 2.68 (t, J=7.2 Hz, 2H), 1.93˜1.86 (m, 2H), 0.61˜0.45 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106021B2
Source datasetuspto-grants-2012_01
ORD IDord-4930e5db82ac4a96af9134c8678c9b83
Source noteuspto-grants-2012_01