HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490067Generated: October 27, 2026
Methanol → 2-Amino-2-[2-(4-benzyloxy-phenyl)-ethyl]-propane-1,3-diol
https://huagongshe.com/reaction/490067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | N-[3-(4-benzyloxy-phenyl)-1,1-bis-hydroxymethyl-propyl]-acetamide | HCID 67054583 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-2-[2-(4-benzyloxy-phenyl)-ethyl]-propane-1,3-diol | HCID 21849131 | — |
Reaction Steps
To a solution of crude N-[3-(4-benzyloxy-phenyl)-1,1-bis-hydroxymethyl-propyl]-acetamide in a mixture of tetrahydrofuran, methanol, water (1/2/2) (450 ml/900 ml/900 ml) is added at room temperature lithium hydroxide (32.7 g, 1.36 mol, 8.0 eq). The reaction mixture is stirred at 55° C. for 5 hours, then extracted with ethyl acetate (500 ml) and washed with brine (2×300 ml), the combined organic layers are then dried with Na2SO4, filtered and concentrated under vacuum. 2-Amino-2-[2-(4-benzyloxy-phenyl)-ethyl]-propane-1,3-diol is isolated after crystallization using ethyl acetate (28.8 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528120B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-7a4a25e1910e41449dc4ff5308c0173b |
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| Source note | uspto-grants-2009_05 |
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