HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004947Generated: October 30, 2026
Carbon tetrabromide → 2-Bromomethyl-3-(2-trimethylsilylethoxymethoxy)-naphthalene
https://huagongshe.com/reaction/1004947
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | [3-(2-Trimethylsilylethoxy-methoxy)-naphthalen-2-yl]-methanol | HCID 22127289 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Bromomethyl-3-(2-trimethylsilylethoxymethoxy)-naphthalene | HCID 22126780 | 65.8% |
Reaction Steps
400 mg (1.30 mmol) of [3-(2-trimethylsilylethoxy-methoxy)-naphthalen-2-yl]-methanol and 462 mg (1.81 mmol) of carbon tetrabromide were dissolved in 5 ml of absolute acetonitrile and the solution was cooled to 0° C. A solution of 446 mg (1.68 mmol) of triphenylphosphine in 6 ml of absolute acetonitrile was added dropwise thereto at 0° C. within 10 minutes and thereafter the mixture was stirred at 0° C. for a further 30 minutes. Subsequently, the solvent was distilled off under reduced pressure and, for purification, the crude product was chromatographed, without further working up, on silica gel using a 2:3 mixture of methylene chloride and hexane as the eluent. There were obtained 314 mg (65% of theory) of 2-bromomethyl-3-(2-trimethylsilylethoxymethoxy)-naphthalene as a light yellow oil; MS: 366, 368 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051712 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-81b67d23a422419690af1bbf686027cc |
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| Source note | uspto-grants-2000_04 |
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