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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635502Generated: October 30, 2026

Ethyl chloroacetate → HCID 70223099, compound

https://huagongshe.com/reaction/635502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium 2-tert-butylphenolateHCID 23680164—
ReactantHCID 86756415HCID 86756415—
ProductHCID 70223099HCID 70223099—

Reaction Steps

The synthesis of this product required the preparation of t-butylphenoxyacetyl chloride from sodium t-butylphenoxide and ethyl chloroacetate. The ethyl t-butylphenoxyacetate obtained is cleaved with potassium hydroxide in order to liberate the t-butylphenoxyacetic acid. The acid chloride is obtained by heating this acid in thionyl chloride. After removing the excess thionyl chloride, the t-butylphenoxyacetyl chloride is reacted with deoxyguanosine according to the procedure described by SCHULHOF et al. for 2-N-phenoxyacetyldeoxyguanosine [Nucleic Acids Res., 15(2), p. 397-415, (1987)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187914B1
Source datasetuspto-grants-2001_02
ORD IDord-f0e45b5caae2421795f409aed45a2bad
Source noteuspto-grants-2001_02