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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096196Generated: October 31, 2026

Potassium bisulfate → 3-[(3,4-Dichloro-phenyl)-(2-hydroxy-ethyl)-amino]-propionic Acid tert-butyl ester

https://huagongshe.com/reaction/1096196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
ReactantLithium borohydrideHCID 4148881—
Reactant3-[(3,4-Dichloro-phenyl)-methoxycarbonylmethyl-amino]-propionic Acid tert-butyl esterHCID 66783134—
Product3-[(3,4-Dichloro-phenyl)-(2-hydroxy-ethyl)-amino]-propionic Acid tert-butyl esterHCID 6678323485.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 7.76 g (21.43 mmol) of 3-[(3,4-dichloro-phenyl)-methoxycarbonylmethyl-amino]-propionic acid tert-butyl ester in 250 ml of ETOH was treated at 0° C. with 0.98 g (42.86 mmol) of LiBH4. The reaction was stirred 10 min at 0° C. and 15 h at RT. After cooling (0° C.) a second batch of 0.49 g (21.43 mmol) of LiBH4 was added and stirred 6 h at RT. The reaction was cooled (0° C.), neutralized with aq. 10% KHSO4 solution and extracted with EtOAc (3×). The organic phase was dried over Na2SO4 evaporated and purified by flash silica gel column (n-heptane:EtOAc 9:1 to 1:1) to yield 6.12 g (85%) of the title compound as light yellow oil. MS: 334.2 (MH+, 2Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138175B2
Source datasetuspto-grants-2012_03
ORD IDord-414e282f6c1942adb86db72b3c2f2a9a
Source noteuspto-grants-2012_03