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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantThionyl ChlorideHCID 24386—
ReactantL-m-tyrosineHCID 6950578—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 2-amino-3-(3-hydroxyphenyl)propanoateHCID 1488869259%

Reaction Conditions

Temperature-5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802666B2
Source datasetuspto-grants-2014_08
ORD IDord-709e1b3ac37e4414a0b30ab88b981d87
Source noteuspto-grants-2014_08