HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403243Generated: October 30, 2026
Benzyl Alcohol → Benzyl 2-amino-3-(3-hydroxyphenyl)propanoate
https://huagongshe.com/reaction/2403243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | L-m-tyrosine | HCID 6950578 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 2-amino-3-(3-hydroxyphenyl)propanoate | HCID 14888692 | 59% |
Reaction Steps
To 10 mL of benzyl alcohol at −5° C. was added, with stirring, 0.2 mL of SOCl2 slowly. The clear colorless solution was cooled to −5° C. and 490 mg of meta-Tyrosine was added. After 5 min, the resulting solution was heated to 120° C. overnight. 100 ml of AcOEt are added. The organic phase are washed with saturated NaHCO3 and brine then dried over Na2SO4, filtered and concentrated to afford 170 as a white solid (430 mg, 59%). 1H NMR (DMSO): δ 1.90 (s, 3H), 2.87 (dd, 1H, J=13.1, 6.5 Hz), 2.94 (dd, 1H, J=13.1, 6.5 Hz), 3.73 (t, 1H, J=6.5 Hz), 5.19 (s, 2H), 6.70 (d, 1H, J=7.7 Hz), 6.75 (s, 1H), 7.17 (t, 1H, J=7.7 Hz), 7.41 (d, 1H, J=7.0 Hz), 7.48 (m, 5H), 9.37 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802666B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-709e1b3ac37e4414a0b30ab88b981d87 |
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| Source note | uspto-grants-2014_08 |
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