HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286333Generated: October 31, 2026
Boron trifluoride etherate → HCID 86737719, compound
https://huagongshe.com/reaction/2286333
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 86737720 | HCID 86737720 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86737719 | HCID 86737719 | 65% |
Reaction Steps
A solution of 1 g (3.7 mmoles) of methyl 2,3,6-trideoxy-4-C-methyl-3-trifluoroacetamido-α-L-lyxo-hexopyranoside (II-A) in 10 ml of dry methylene dichloride was treated at -70° with 0.05 ml of boron trifluoride etherate. While maintaining the temperature at -70°, an excess of diazomethane dissolved in methylene dichloride was added until a faint yellow color persisted. After 60 minutes at -70°, a white solid (polymethylene) was removed by filtration, and the filtrate was washed successively with 10% sodium bicarbonate solution and with water, after which it was dried with anhydrous magnesium sulfate. The residue which was obtained by evaporation was chromatographed on a silica-gel column. Elution with a 95:5 chloroform:acetone mixture gave pure methyl 2,3,6-trideoxy-4-C-methyl-4-O-methyl-3-trifluoroacetamido-α-L-lyxo-hexopyranoside (II-B, 0.68 g, 65%) as a syrup; [α]D =-129° (c=1.1 in CHCl3); mass spectrum m/e 285 (M+). The pmr spectrum (CDCl3) showed absorptions at 1.22 (s, CH3 -C-4), 1.28 (d, CH3 -C-5), 3.33 and 3.48 (two s, --OCH3) and 4.77δ (broad s, C-1-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04265885 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-09db852619da4f27bd869ef13e5be9d4 |
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| Source note | uspto-grants-1981_05 |
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