Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655682Generated: October 25, 2026

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

https://huagongshe.com/reaction/1655682

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 numberUS05250720
Source datasetuspto-grants-1993_10
ORD IDord-abe011cb3b3a40019232e414a44c4e89
Source noteuspto-grants-1993_10