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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616685Generated: October 31, 2026

Thionyl Chloride → HCID 178440617, compound

https://huagongshe.com/reaction/1616685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178427878HCID 178427878—
Solventtert-ButanolHCID 6386—
ProductHCID 178440617HCID 178440617—

Reaction Conditions

Temperature-10 °C

Reaction Steps

SOCl2 (1 mL) is added dropwise to a solution of cis-4-[(2R,6S)-10-hydroxy-6,11,11-trimethyl-1,2,5,6-tetrahydro-4H-2,6-methano-benzo[d]azocine-3-carbonyl]-cyclohexane carboxylic acid (100 mg) in tert-butanol (5 mL) cooled to −10° C. Then, the cooling bath is removed and the resulting solution is stirred at ambient temperature overnight before another portion of SOCl2 (1 mL) is added. After stirring for additional 12 h more SOCl2 (2 mL) is added and the solution is heated to 50° C. The solution is stirred at this temperature for 48 h before HCl in 1,4-dioxane (1 mL) is added. The resulting solution is stirred at reflux temperature overnight and then treated with concentrated H2SO4 (3 mL). After stirring at reflux temperature for additional 3 h, the solution is cooled to ambient temperature and concentrated under reduced pressure. The residue is treated with water and the precipitate is separated by filtration. The precipitate is taken up in ethyl acetate and washed with water and dried (MgSO4). After removing the solvent, the residue is purified by HPLC (water/MeCN/F3CCO2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765780B2
Source datasetuspto-grants-2014_07
ORD IDord-087ec9cad268484282f5f161a1c8b71b
Source noteuspto-grants-2014_07