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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243828Generated: November 1, 2026

Phenacyl bromide → HCID 14308410, compound

https://huagongshe.com/reaction/2243828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantN-tert-Butoxycarbonyl-L-threonineHCID 2724766—
SolventEthyl AcetateHCID 8857—
ProductHCID 14308410HCID 1430841085%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred suspension of Boc-Thr-OH (21.91 g, 0.1 mol) in EtOAc (200 ml) at 0° C., TEA (14 ml, 0.1 mol) and bromoacetophenone (19.0 g, 0.1 mol) were added. The reaction mixture was allowed to warm to 20° C., stirred for 2 days and then diluted with EtOAc (500 ml). After washing successively with aq HCl (200 ml, 0.1 N), H2O (100 ml), aq NaHCO3 (200 ml, 1 N) and brine (200 ml), drying (Na2SO4), filtered and concentrated in vacuo, the residue was triturated with Et2O and filtered. The resulting solid was dried in the dark to yield D3 (28.6 g, 85%). Rf=0.55 (hex-EtOAc 1:1, silica); M.p.=114.2° C.; [α]D22−29.4 (c 2, EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678765B2
Source datasetuspto-grants-2010_03
ORD IDord-8b51bdcbf7364479a93fbd6f65418f4a
Source noteuspto-grants-2010_03