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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286333Generated: October 31, 2026

Boron trifluoride etherate → HCID 86737719, compound

https://huagongshe.com/reaction/2286333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantDiazomethaneHCID 9550—
ReactantHCID 86737720HCID 86737720—
SolventDichloromethaneHCID 6344—
ProductHCID 86737719HCID 8673771965%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04265885
Source datasetuspto-grants-1981_05
ORD IDord-09db852619da4f27bd869ef13e5be9d4
Source noteuspto-grants-1981_05