HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386845Generated: October 30, 2026
Hydrochloric Acid → 4-(2,4-Bis(methoxymethoxy)phenyl)tetrahydrothio-pyran-4-ol
https://huagongshe.com/reaction/386845
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Tetrahydrothiopyran-4-one | HCID 66173 | — |
| Reactant | 1-Bromo-2,4-bis(methoxymethoxy)benzene | HCID 11391754 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(2,4-Bis(methoxymethoxy)phenyl)tetrahydrothio-pyran-4-ol | HCID 66745159 | — |
Reaction Steps
6.35 ml of tetramethylethylenediamine are added to a solution of 5.54 g of 1-bromo-2,4-bis(methoxy-methoxy)benzene in 80 ml of tetrahydrofuran. The mixture is cooled to −70° C. and 16.8 ml of 2.5M n-butyllithium in hexane are added. The reaction medium is stirred at −70° C. for 1 hour and 2.79 g of tetrahydrothiopyran-4-one in solution in 30 ml of tetrahydrofuran are added. The reaction medium is stirred at −70° C. for 1 hour and then left at ambient temperature overnight. 50 ml of 2M hydrochloric acid are added and the reaction medium is vigorously stirred for 15 minutes and then extracted with ethyl acetate. The organic phases are combined, washed with a saturated solution of sodium chloride, dried over magnesium sulphate and evaporated. The residue is chromatographed on silica gel, elution being carried out with a 75/25 mixture of heptane/ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372879B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-81ba2ea0078846ec9d369199fbe3e890 |
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| Source note | uspto-grants-2013_02 |
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