HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620524Generated: October 31, 2026
Acetic Acid → (+-)(2R*,3R*)-2-amino-2-methyl-1,3-butanediol acetate
https://huagongshe.com/reaction/620524
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | (+-)(2R*,3R*)-2-Methyl-2-nitro-1,3-butanediol | HCID 13375425 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (+-)(2R*,3R*)-2-amino-2-methyl-1,3-butanediol acetate | HCID 86741969 | — |
Reaction Steps
To a solution of (+-)(2R*,3R*)-2-methyl-2-nitro-1,3-butanediol (20B, 22.1 g, 0.148 mol) in 95% EtOH (150 mL) was added glacial acetic acid (25 mL) and 10% Pd/C (MCB, 2.0 g). The reduction was carried out in a Parr apparatus at 50 psi of H2 during a 48 h period at RT. The catalyst was removed by filtration through a Millipore® filter, and the solvent removed under vacuum (2 days). The viscous, colorless syrup was dissolved in abs. EtOH (30 mL). Dilution with abs. Et2O (300 mL) give a cloudy liquid which was placed in a refrigerator for two days. During this time, colorless crystals formed which were washed with Et2O and dried in a vacuum oven at RT for two days. The yield of (+-) (2R*,3R*)-2-amino-2-methyl-1,3-butanediol acetate was 25.6 g (97%) mp 117°-121°, (C, H, N).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04820873 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-bc3f6017e67745a4bee12e7c14ab4e7d |
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| Source note | uspto-grants-1989_04 |
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