HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59217Generated: October 30, 2026
(Diethylamino)sulfur trifluoride → HCID 67153916, compound
https://huagongshe.com/reaction/59217
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 67153941 | HCID 67153941 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67153916 | HCID 67153916 | 7% |
Reaction Steps
To a solution of {(1S,2S,3S,4R,5S)-2,3,4-Tris-benzyloxy-5-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-6,8-dioxa-bicyclo[3.2.1]oct-1-yl}-methanol (616 mg, 0.871 mmol) in dichloromethane (3 mL) at 0 degrees Celsius was added diethylaminosulfur trifluoride (170 microL, 1.3 mmol) and the resulting mixture was slowly warmed to room temperature and stirred at this temperature for 16 hours. The mixture was diluted with dichloromethane and washed with a saturated solution of aqueous sodium bicarbonate, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography over silica gel using a 40 g redisep silica cartridge (eluting with a gradient of 0 to 20% ethyl acetate in heptane) to afford (1S,2S,3S,4R,5S)-2,3,4-tris-benzyloxy-5-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-1-fluoromethyl-6,8-dioxa-bicyclo[3.2.1]octane as a colorless oil (40 mg, 7% yield). (LCMS) 753.4 (M+HCOO−: negative mode).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09439902B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-2b07358abe594217b1429f6c3ad40488 |
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| Source note | uspto-grants-2016_09 |
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