HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16346Generated: October 25, 2026
Toluene → (S)-5-benzyloxymethylmorpholin-3-one
https://huagongshe.com/reaction/16346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | 2-Amino-3-(benzyloxy)propan-1-ol | HCID 14118408 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-5-benzyloxymethylmorpholin-3-one | HCID 67077731 | — |
Reaction Steps
Bromoacetyl chloride (5.06 mL) was added to a solution mixture of toluene (100 mL) and a 2 N sodium hydroxide aqueous solution (100 mL) of (R)-(+)-2-amino-3-benzyloxy-1-propanol (10 g) under ice-cooling. The resulting reaction solution was stirred at 0° C. for 30 min and then further stirred at 60° C. for 1 hr. The reaction solution was cooled to room temperature, and a solution mixture of toluene and THF (1:1) was added thereto. The organic layer was separated, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system) to give 1.36 g of the title compound. The physical property values of this compound were as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737141B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-0de979c1ecc44607a3376da65e857d14 |
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| Source note | uspto-grants-2010_06 |
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