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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375725Generated: November 1, 2026

Diisopropylethylamine → 3-(4-Tert-butoxycarbonylaminophenyl)propanol

https://huagongshe.com/reaction/1375725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-{[(Tert-butoxy)carbonyl]amino}phenyl)propanoic acidHCID 17040111—
SolventTetrahydrofuranHCID 8028—
SolventEthylacetate heptaneHCID 21899848—
Product3-(4-Tert-butoxycarbonylaminophenyl)propanolHCID 2199401349%

Reaction Steps

3-{4-[(tert-Butoxycarbonyl)amino]phenyl}propanoic acid (1.33 g, 5.013 mmol) and BOP reagent (2.882 g, 6.517 mmol) were mixed in THF (30 ml). DIPEA (907 mg, 7.018 mmol) was added. The mixture was stirred for 10 minutes. Sodium borohydride (246 mg, 6.517 mmol) was added. The mixture was stirred for 30 minutes more and then evaporated to dryness. Ethyl acetate and water were added into the residue. The organic phase was washed with water and brine and dried with magnesium sulfate. The solvent was evaporated and an oil mixture was obtained. Column chromatography of the oil on silica gel using ethyl acetate/heptane (10:90, then 25:75) as eluant gave the desired oil product (616 mg), yield 49%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169810B2
Source datasetuspto-grants-2007_01
ORD IDord-976cd2dc782f42449d27f983e2fed0a0
Source noteuspto-grants-2007_01