HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918268Generated: November 1, 2026
Methanesulfonic Acid → HCID 21521870, compound
https://huagongshe.com/reaction/918268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Butyl vinyl ether | HCID 8108 | — |
| Reactant | HCID 68145100 | HCID 68145100 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21521870 | HCID 21521870 | — |
Reaction Steps
Contacting (1S, 2S, 5S) -5-(1,2,3,4 -tetrahydro-6-methoxy-2-naphthyl)-2-hydroxy-1-methylcyclopentaneacetic acid with butyl vinyl ether in THF containing methanesulfonic acid affords the stereochemically corresponding α-butoxyethyl 2-(α-butoxyethoxy)-5-(1,2,3,4-tetrahydro-6-methoxy-2-naphthyl)-1 -methylcyclopentaneacetate, in which the ester linkage is cleaved and the carboxyl reduced to hydroxy by contacting with lithium tetrahydroaluminate (1-) in THF. From the resultant alcohol, on esterification with acid chloride or anhydride in pyridine, followed by cleavage of the ether linkage via hydrochloric acid in acetone, the corresponding mono ester of the invention wherein the ester grouping is on the ethanolic side chain eventuates. Contacting such a mono ester with acid chloride or anhydride affords a di-ester of the invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03970686 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-f54557fec1d9426bb4adfd54801cb191 |
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| Source note | uspto-grants-1976_07 |
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