HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247679Generated: October 31, 2026
Carbon tetrabromide → HCID 86620175, compound
https://huagongshe.com/reaction/1247679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl (4-mercapto-2-methylphenoxy)acetate | HCID 16641178 | — |
| Reactant | HCID 86209014 | HCID 86209014 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86620175 | HCID 86620175 | 33.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129268B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-2cdf02f40bae4c469402c4a9496a9334 |
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| Source note | uspto-grants-2006_10 |
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