HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653757Generated: October 30, 2026
2,6-Anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate → HCID 15699249, compound
https://huagongshe.com/reaction/653757
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Anhydro-5-deoxy-D-arabino-hex-5-enitol triacetate | HCID 640125 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | 4-Penten-1-OL | HCID 13181 | — |
| Product | HCID 15699249 | HCID 15699249 | 123.2% |
Reaction Steps
A solution of 3,4,6-tri-O-acetyl-D-galactal (3.6 g) in acetonitrile (40 ml) anhydrous lithium bromide (4.7 g), 4-pentene-1-ol (4 ml), molecular sieves 4 Å (4 g) and the activated resin prepared as in Example 1 (5.1 g) was stirred at room temperature for 30 min. The product was isolated as described in Example 1 and purified on a column of Silica Gel using ethyl acetate-hexane (1:6) as eluant and yielded the title compound (2.92 g) and minor β-glycoside (0.32 g). [α]D20 (α-anomer)=+126°±2° (c 1.03, CHCl3); [α]D20 (β-anomer)=-9.4°±2° (c 1.03, CHCl3) 1H NMR δ (α anomer): 5.81 (m, --CH=C), 5.33 (d, H-1), 5.28 (m, H-3), 4.94-5.06 (m, H-4, C=CH 2), 4.16-4.06 (H-6a,b, H-5), 3.65 and 3.40 (m, O-CH2 -), 2.1 (m, H-2eq), 1.86 (m, H-2ax) MS (calc. mass for C17H26O8 =358.17). Obs. m/e 571.33, 357.21, 299.19, 273.05, 213.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05128463 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-4e256e5d9eeb40fa802157043b30499e |
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| Source note | uspto-grants-1992_07 |
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