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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247679Generated: October 31, 2026

Carbon tetrabromide → HCID 86620175, compound

https://huagongshe.com/reaction/1247679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl (4-mercapto-2-methylphenoxy)acetateHCID 16641178—
ReactantHCID 86209014HCID 86209014—
SolventDichloromethaneHCID 6344—
ProductHCID 86620175HCID 8662017533.2%

Reaction Steps

A solution of tetrabromomethane (2.1 g, 6.6 mmol) in dry methylene chloride (20 mL) was added dropwise to an ice-cooled solution of 3-(4-bromophenyl)-3-iodoprop-2-en-1-ol (1.5 g, 4.4 mmol) and triphenylphosphine (2.4 g, 9.0 mmol) in dry methylene chloride (50 mL). The reaction mixture was stirred at room temperature for 2 h and the solvent was evaporated in vacuo. Under nitrogen atmosphere, N,N-diisopropylethylamine (1.2 g, 9.0 mmol) and ethyl (4-mercapto-2-methylphenoxy)acetate (1.5 g, 6.6 mmol; Bioorg. Med. Chem. Lett. 2003, 13, 1517) were added to the residue. The reaction mixture was stirred for 3 h, filtered through a short path of silica gel and the filtrate was evaporated in vacuo. The residue was purified by column chromatography (silica gel Merck 60, hexane/ethyl acetate 1:0–9:1) giving 0.80 g of the ester. Yield: 0.80 g (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129268B2
Source datasetuspto-grants-2006_10
ORD IDord-2cdf02f40bae4c469402c4a9496a9334
Source noteuspto-grants-2006_10