Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081968Generated: October 27, 2026

N-(tert-butoxycarbonyl)glycine → Boc-Gly-Leu-Ala-OBzl

https://huagongshe.com/reaction/2081968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantH-Leu-Ala-OBzlHCID 16742166—
ProductBoc-Gly-Leu-Ala-OBzlHCID 131717744—

Reaction Steps

Boc-Gly-Leu-Ala-OBzl was prepared by coupling Boc-Gly-OH (5.70 g, 32.6 mmoles) to H-Leu-Ala-OBzl using the mixed anhydride procedure described in Example 2. The product (13.8 g) was obtained as an amorphous solid. Boc-Gly-Leu-Ala-OBzl was deblocked with trifluoroacetic acid by the procedure described for the preparation of H-Leu-Ala-OBzl except that the trifluoroacetate salt was soluble in ether. The preparation was dissolved in ethyl acetate and treated with anhydrous hydrogen chloride. The resulting product was precipitated by the addition of ether to yield 7.7 g of H-Gly-Leu-Ala-OBzl .HCl in a first crop.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187157
Source datasetuspto-grants-1993_02
ORD IDord-7e4a199de4244e5a88abb9c20f9c36ff
Source noteuspto-grants-1993_02