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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059085Generated: November 2, 2026

Hydrochloric Acid → HCID 13096683, compound

https://huagongshe.com/reaction/2059085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2,2-Dimethyl-3-(thiophen-2-yl)propanoic acidHCID 10487746—
CatalystWaterHCID 962—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 13096683HCID 13096683—

Reaction Steps

A solution of 2,2-dimethyl-3-(2-thienyl)propanoic acid (Va; 11.2 g., 0.06 mole), diphenylphosphorylazide (16.7 g., 0.06 mole) (Aldrich Chemical Company), and triethylamine (6.14 g., 0.06 mole) in tert.-butanol (100 ml.) was heated at reflux for 5 hr. The solution was poured into water (300 ml.) and the crude material extracted with Et2O. The combined extracts were washed with brine, dried over MgSO4 and finally evaporated to get 11.9 g. of crude intermediate. This oil was added to a mixture of ethylene glycol (50 ml.), H2O (20 drops) and KOH (10 g.). The mixture was heated at reflux for 5 hr., cooled to 25°, diluted with H2O (300 ml.) and acidified to pH 1 with conc. HCl. A wash with Et2O removed the acid insoluble material which was discarded. The aqueous solution was made basic with 50% NaOH and the product was extracted with Et2O. The ether extracts were washed with brine, dried over a MgSO4 and evaporated to give 6.9 g. (74%) of product. the NMR spectrum is consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04321398
Source datasetuspto-grants-1982_03
ORD IDord-07dfbf98f42b44e09ecbaeb0775224d9
Source noteuspto-grants-1982_03