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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882144Generated: October 30, 2026

Hydrochloric Acid → 2-(((tert-Butyldimethylsilyl)oxy)methyl)acrylic acid

https://huagongshe.com/reaction/882144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantLithium 2-(hydroxymethyl)prop-2-enoateHCID 89613527—
SolventDimethylformamideHCID 6228—
Product2-(((tert-Butyldimethylsilyl)oxy)methyl)acrylic acidHCID 44604257—

Reaction Steps

To lithium 2-(hydroxymethyl)prop-2-enoate (926 mg, 8.57 mmol) was added DMF (17.0 mL), HCl (1.07 mL, 4 M in dioxanes, 4.28 mmol) and imidazole (700 mg, 10.3 mmol), followed by TBS-Cl (2.84 g, 18.9 mmol) at 25° C. The reaction was stirred overnight, then quenched by pouring into a separatory funnel containing water. The aqueous layer was brought to pH˜3 with 1 N HCl and was extracted with ethyl acetate (×3). The organic layers were combined and dried with Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by chromatography using MPLC using 5-80% EtOAc/hexanes. The monoprotected product was collected and concentrated in vacuo to afford a clear oil. 1H NMR (600 MHz, DMSO-D6) δ 12.67 (s, 1H), 6.13 (s, 1H), 5.80 (s, 1H), 4.31 (s, 2H), 0.92 (s, 9H), 0.09 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993756B2
Source datasetuspto-grants-2015_03
ORD IDord-512b8cdb14a048e8b47cf13463230c96
Source noteuspto-grants-2015_03