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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260762Generated: October 25, 2026

Nitrogen → Z-Thr(tBu)-OtBu

https://huagongshe.com/reaction/2260762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSulfuric AcidHCID 1118—
ReactantIsobutyleneHCID 8255—
ReactantN-((Benzyloxy)carbonyl)-L-threonineHCID 88217—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductZ-Thr(tBu)-OtBuHCID 72698559—

Reaction Conditions

Temperature20 °C

Reaction Steps

Z-Thr-OH (25.3 g, 0. 1 mol, Peptide Research Laboratories, Japan) was suspended in dichloromethane (250 ml), to which was added conc. sulfuric acid (1 ml). The mixture was cooled on a dry ice-acetone bath, to which was blown isobutene (the volume increased by 200 ml). The vessel was closed tightly, and the mixture was stirred for 2 days at 20° C. The vessel was opened, into which was blown N2 at 20° C. to purge isobutene, followed by addition of water. The mixture was neutralized with a 10% (W/V) aqueous solution of sodium hydrogencarbonate, which was subjected to extraction twice with dichloromethane. The dichloromethane layer was dried over anhydrous sodium sulfate, then the solvent was distilled off. The residue was purified by means of a silica gel column chromatography (n-hexane:chloroform =1:2) to give an oily product. The yield was 26.6 g (72.7%). Rf: 0.21 (n-hexane:chloroform =1:2) FAB-MS (M+H+)=366 (Theoretical value =366)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478809
Source datasetuspto-grants-1995_12
ORD IDord-91fb7d45e2dd4becbc4f2147baef1240
Source noteuspto-grants-1995_12