HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483014Generated: October 25, 2026
Methanesulfonyl chloride → 5-Phenyl-2-pentanol mesylate
https://huagongshe.com/reaction/483014
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-Hydroxy-1-phenylpentane | HCID 102788 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Phenyl-2-pentanol mesylate | HCID 12878386 | 95% |
Reaction Steps
To a stirred solution of 5-phenyl-2-pentanol (482 g.; 2.94 moles) in tetrahydrofuran (2250 ml.) at 0° C. was added methanesulfonyl chloride (300 ml.) at such a rate that the internal temperature does not rise above 10° C. (total addition time 4.5 hours). After addition is complete, the reaction mixture was allowed to warm to room temperature and stirring was continued for an additional hour. The reaction mixture was filtered and the supernate concentrated to a light yellow oil (2800 g.) which was dissolved in chloroform (2 liters) and washed with water (4×1 liter), brine (1×1 liter), charcoal treated (50 g.), dried (MgSO4), filtered through diatomaceous earth and concentrated to a light orange oil (687 g., 95% yield). This material was suitable for use without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04576964 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-1e96217cc56547018a5b14e6a4ab7384 |
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| Source note | uspto-grants-1986_03 |
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