HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891671Generated: October 30, 2026
Tetrahydrofuran → HCID 69544082, compound
https://huagongshe.com/reaction/891671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 131725362 | HCID 131725362 | — |
| Product | HCID 69544082 | HCID 69544082 | 100% |
Reaction Steps
To a solution of 3-t-butyldiphenyloxy-1-{4-[2-(t-butyldiphenylsilyloxy)-1-(t-butyldiphenylsilyloxymethyl)ethylcarbamoyl]-1,3-thiazol-2-yl}azetidine (3.19 g, 3.23 mmol) (obtained as described in Reference Example 39(3)) in anhydrous tetrahydrofuran (160 ml) was added a solution of 1.0M tetra-n-butylammonium fluoride in tetrahydrofuran (11.6 ml, 11.6 mmol) in an ice bath. The mixture was stirred in the ice bath for 2 hours. After checking the completion of the reaction, the reaction mixture was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using ethyl acetate:methanol (9:1→8:2) as the eluant to afford 3-hydroxy-1-{4-[2-hydroxy-1-(hydroxymethyl)-ethylcarbamoyl]-1,3-thiazol-2-yl}azetidine (1.21 g, yield 100%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-c4bbe5d38cf9424d8a1e404fb32aa2c3 |
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| Source note | uspto-grants-2006_02 |
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