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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | 3-[(3,4-Dichloro-phenyl)-methoxycarbonylmethyl-amino]-propionic Acid tert-butyl ester | HCID 66783134 | — |
| Product | 3-[(3,4-Dichloro-phenyl)-(2-hydroxy-ethyl)-amino]-propionic Acid tert-butyl ester | HCID 66783234 | 85.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138175B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-414e282f6c1942adb86db72b3c2f2a9a |
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| Source note | uspto-grants-2012_03 |
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