HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434070Generated: October 31, 2026
(Diethylamino)sulfur trifluoride → HCID 23594044, compound
https://huagongshe.com/reaction/434070
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 9944398 | HCID 9944398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23594044 | HCID 23594044 | 56% |
Reaction Steps
To a solution of diethylaminosulfur trifluoride (0.073 mL, 0.45 mmol) in CH2Cl2 (2 mL) cooled at −78° C. in a flame-dried flask under argon was added dropwise a solution of 6C (92 mg, 0.3 mmol) in CH2Cl2 (12 mL). After addition, the reaction mixture was stirred at −78° C. for 30 min, then at 0° C. overnight. The reaction mixture was partitioned between CH2Cl2 and saturated aqueous NaHCO3. The separated aqueous layer was extracted with CH2Cl2 (2×). The combined CH2Cl2 layers were washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated under reduced pressure to give a crude product, which was chromatographed (silica gel) eluting with EtOAc/hexane (1:2) to give 52 mg of the title compound (racemate) as a white solid. m.p. 228-230° C.; HPLC: 99% at 5.0 min (retention time) (Conditions: Zorbax SB C18 (4.6×75 mm); Eluted with 0% to 100% B, 8 min gradient. (A=90% H2O−10% MeOH−0.1% H3PO4 and B=10% H2O−90% MeOH−0.1% H3PO4); Flow rate at 2.5 mL/min. UV detection at 220 nm). MS (ES): m/z 641 [2M+Na]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670386B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-9dc39e13c0144cd5994cb2ea6b2e02b9 |
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| Source note | uspto-grants-2003_12 |
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