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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764785Generated: November 3, 2026

Hydrochloric Acid → Boc-Thr(Bzl)-Ser(Bzl)-Ser(Bzl)-Glu(OBzl)-OH

https://huagongshe.com/reaction/1764785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantBoc-Thr(Bzl)-OSuHCID 12879029—
ReactantBoc-Ser(Bzl)-Ser(Bzl)-Glu(OBzl)-OHHCID 131711277—
SolventDimethyl SulfoxideHCID 679—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductBoc-Thr(Bzl)-Ser(Bzl)-Ser(Bzl)-Glu(OBzl)-OHHCID 131711276—

Reaction Steps

Boc-Ser(Bzl)-Ser(Bzl)-Glu(OBzl)-OH (71.6 g, 104 mmol) was treated with 2.7 liters of freshly prepared 3.9 N HCl in THF for 45 minutes. The mixture was evaporated to dryness and the residue evaporated twice more with THF to give a solid mass (59.3 g; mp 161°-165°). It was collected and washed with ether and stirred in 500 ml of DMF with Boc-Thr(Bzl)-OSu (38.2 g, 94 mmol) in the presence of Et3N (25 ml) at 0° for 1 hour and then at 25° for 15 hours. More Et3N (14.5 ml) was added in several portions during this time to maintain the reaction slightly basic. Some insoluble matter formed was filtered off and the filtrate evaporated to an oil which was dissolved in EtOAc (1.5 liters), washed with 5% HOAc, H2O (2 times), dried (Na2SO4), and evaporated to a solid mass. The product was recrystallized from EtOAc and petroleum ether to yield, 64.8 g (78.1%); mp 115°-118°; [α]D25 = +11.64° (c l, DMSO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116951
Source datasetuspto-grants-1978_09
ORD IDord-1cb1b0ce09144a25a1d92d96401c4ab2
Source noteuspto-grants-1978_09