HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520430Generated: October 31, 2026
(Bis(2-methoxyethyl)amino)sulfur trifluoride → HCID 89686732, compound
https://huagongshe.com/reaction/520430
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Bis(2-methoxyethyl)amino)sulfur trifluoride | HCID 2734690 | — |
| Reactant | HCID 86690128 | HCID 86690128 | — |
| Product | HCID 89686732 | HCID 89686732 | 63% |
Reaction Steps
Neat Deoxo-Fluor® (342 mg, 1.546 mmol) was added to a cold (0° C.) stirred ethyl 2-(hydroxymethyl)tetrahydro-2H-pyran-2-carboxylate (194 mg, 1.031 mmol) and the mixture was heated at 70° C. overnight. The reaction was quenched with ice and neutralized with sat. aq. NaHCO3 and extracted with DCM (2×). The combined organic layers were washed with water, brine and dried (MgSO4), filtered and dried to give a yellow-orange oil which was purified by silica gel FCC (0-5% EtOAc in DCM) to afford ethyl 2-(fluoromethyl)tetrahydro-2H-pyran-2-carboxylate as a colorless oil (125 mg, 63%) which was saponified (LiOH.H2O, MeOH-THF—H2O, sonicate) to afford Cap P-43 as a viscous oil (82 mg, 77%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 4.66-4.54 (m, 1H), 4.54-4.41 (m, 1H), 4.02-3.84 (m, 2H), 1.98-1.84 (m, 1H), 1.84-1.72 (m, 2H), 1.69-1.52 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09326973B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-912978ccb3c74fa9a04f311ea8cbdfb0 |
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| Source note | uspto-grants-2016_05 |
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