Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzenemethanol, .alpha.-ethyl-4-methoxy- | HCID 92218 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Methoxyphenyl)-1-propanol | HCID 79406 | — |
| Product | Methanesulfonate | HCID 85257 | 421.2% |
Reaction Steps
Methyl sulphonyl chloride (12.5 g, 0.11M) was added dropwise to a stirred solution of p-methoxyphenylpropanol (16.6 g, 0.10M) in dichloromethane (60 ml)/pyridine (20 ml) at 0° C. The reaction mixture was maintained at 0° C. for 12 hours, then diluted with dichloromethane (250 ml) and washed with hydrochlorid acid (5×50 ml of 5M.1-1). The solution was washed with water, dried (MgS04) and the solvent was evaporated off under reduced pressure to give 3-(4-methoxyphenyl)propan-1-ol, methane sulphonate (20 g), as a colourless crystalline solid, m.p. 41-42° C. (pentane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04636518 |
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| Source dataset | uspto-grants-1987_01 |
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| ORD ID | ord-6c1ed3ff96d344dabadb5b5bd68ecafc |
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| Source note | uspto-grants-1987_01 |
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