HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199272Generated: October 25, 2026
Aldono-1,5-lactone → 1-C-(1,3-dithian-2-yl)-D-glucopyranose
https://huagongshe.com/reaction/1199272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aldono-1,5-lactone | HCID 736 | — |
| Reactant | 1-C-[bis(methylthio)methyl]-D-glucopyranose | HCID 53998654 | — |
| Reactant | HCID 178506910 | HCID 178506910 | — |
| Product | 1-C-(1,3-dithian-2-yl)-D-glucopyranose | HCID 54279519 | — |
Reaction Steps
Process 1", i.e. a process to produce, for example, 1-C-[bis(methylthio)methyl]-D-glucopyranose derivative (2") from D-glucono-δ-lactone derivative (1"), is conducted by allowing the compound (1") to react with bis(methylthio)methyllithium, or a process to produce 1-C-(1,3-dithian-2-yl)-D-glucopyranose (2"), is conducted by allowing the compound (1") to react with 2-lithio-1,3-dithiane. In this reaction, usually 1 to 5 mole equivalents, preferably 2-2.5 mole equivalents, of bis(methylthio)methyllithium or 2-lithio-1,3-dithiane for D-glucono-δ-lactone derivative (1") is used. This reaction is conducted in an appropriate solvent which is inactive to this reaction, such as tetrahydrofuran, 1,4-dioxane, ethyl ether, and hexane, which are used separately or in combination, preferably in an atmosphere of an inert gas such as nitrogen and argon. Reaction temperature is usually -20° C.--78° C., preferably -50° C.--78° C. in the initial stage of the reaction and -20° C.--40° C. in the later stage. Reaction time is appropriately about 1-8 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04898986 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-103ebd841cd34bc9a6cbedb1a7633ec9 |
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| Source note | uspto-grants-1990_02 |
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