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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370004Generated: October 30, 2026

Pivaloyl chloride → HCID 135986991, compound

https://huagongshe.com/reaction/1370004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 136341215HCID 136341215—
SolventPyridineHCID 1049—
ProductHCID 135986991HCID 13598699158%

Reaction Steps

To a solution of N2-monomethoxytrityl-9-(4-hydroxy-3-hydroxymethylbut-1-yl)guanine (0.47 g, 0.9 mmol) in pyridine (4.5 ml) was added pivalyl chloride (0.55 ml, 4.5 mmol) and the solution was stirred for 45 minutes. The mixture was precipitated in water (45 ml) and the resulting precipitate was stirred in 80% acetic acid (10 ml) at 80° for 20 minutes. The solvent was removed and the residue was purified by column chromatography on silica gel eluting with chloroform-methanol (10:1) to afford 9-(4-pivalyloxy-3-pivalyloxymethylbut-1-yl)guanine (0.22 g, 58%), m.p. 225-237° C.; νmax (KBr) 3430, 2980, 1730, 1690, and 1620 cm−1; δH [(CD3)2SO] 1.11 (18H, s, 2×C(CH3)3), 1.81 (2H, q, J 6.8 Hz, 2′-H), 1.93 (1H, m, 3′-H), 4.0-4.1 (6H, m, 1′-H and 2×4′-H), 6.38 (2H, s, 2-NH2), 7.69 (1H, s, 8-H), and 10.58 (1H, br.s, 1-H); (Found: C, 56.58; H, 7.26; N, 16.14%; C20H31N5O5 requires: C, 56.99; H, 7.41; N, 16.62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579981B1
Source datasetuspto-grants-2003_06
ORD IDord-0b093867595a4f098bd530a7656206ca
Source noteuspto-grants-2003_06