Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | D-Arabinose | HCID 66308 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-Benzyl-D-arabinose | HCID 86616725 | — |
Reaction Steps
D-Arabinose (50 kg, 330.04 moles) and benzyl alcohol (132.2 kg, 4.33 equivalents) were stirred and heated to 35° C. Acetyl chloride (10.9 kg, 0.42 equivalents), keeping the temperature <45° C., then stirred 50° C. overnight. The mixture was cooled to 20° C. and diluted with MTBE (600 kg). The mixture was stirred for 0.5−5 h. The solids were collected by filtration and washed with MTBE (2×40 kg). The material was dried in a filter drier. 2-Benzyl-D-arabinose was obtained as an off-white solid, 70.9 kg (88.6%). 1H NMR (300 MHz, DMSO-d6): δ 7.32 (m, 5H), 4.76 (s, 1H), 4.66 (d, J=12 Hz, 1H), 4.59 (m, 3H), 4.45 (d, J =12 Hz, 1H), 3.70 (m, 4H), 3.47(dd, J=12, 3 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501439B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-30f01609220f49bf9ce6795f15a73cfa |
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| Source note | uspto-grants-2009_03 |
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