HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440945Generated: October 29, 2026
Triethylamine → 1-Methylsulfonyloxy-5-phenylpentane
https://huagongshe.com/reaction/440945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5-Phenyl-1-pentanol | HCID 61523 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methylsulfonyloxy-5-phenylpentane | HCID 11630107 | 99.9% |
Reaction Steps
A stirred solution of 25.0 grams (0.152 mole) of 5-phenylpentanol and 23.3 mL (0.167 mole) of triethylamine in 250 mL of methylene chloride was cooled to 0° C., and a solution of 13.0 mL (0.167 mole) of methanesulfonyl chloride in 50 mL of methylene chloride was added dropwise at a rate to maintain the reaction mixture temperature at 0° C. to 5° C. The complete addition required about 45 minutes. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature. After this time the reaction mixture was washed with two 200 mL portions of an aqueous 5% sodium bicarbonate solution and then with 200 mL of an aqueous solution saturated with sodium chloride. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 36.8 grams of 1-methylsulfonyloxy-5-phenylpentane. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521192 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-7d3c707f4c8e49e382b562cc81ac93b0 |
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| Source note | uspto-grants-1996_05 |
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