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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4983Generated: October 26, 2026

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

https://huagongshe.com/reaction/4983

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 numberUS05242904
Source datasetuspto-grants-1993_09
ORD IDord-e95bb68602144d5c8b548570c446fb1d
Source noteuspto-grants-1993_09