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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405745Generated: October 31, 2026

tert-Butanol → (2-Phenylhexahydro-2,5-methanopentalen-3a-yl)carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2405745

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-Phenylhexahydro-2,5-methanopentalene-3a-carboxylic acidHCID 67300718—
Product(2-Phenylhexahydro-2,5-methanopentalen-3a-yl)carbamic acid tert-butyl esterHCID 68310785—

Reaction Steps

2-Phenylhexahydro-2,5-methanopentalen-3a-carboxylic acid (50 g) was dissolved in t-butanol (1 l), and triethylamine (51 g) was added to this solution. Diphenylphosphoryl azide (56 g) was added in portions at room temperature. The reaction was stirred first at room temperature and then at reflux. After removal of the t-butanol, the residue was taken up in water (800 ml). The precipitated solids were filtered off and washed repeatedly with water. After drying under reduced pressure, the solids were taken up in tert-butyl methyl ether. This forms a solid, which was filtered off. The filtrate was concentrated fully under reduced pressure and then stirred with diisopropyl ether. The solids were filtered off with suction and washed with a mixture of diisopropyl ether and n-heptane. After drying, (2-phenylhexahydro-2,5-methanopentalen-3a-yl)carbamic acid tert-butyl ester (83.9 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809325B2
Source datasetuspto-grants-2014_08
ORD IDord-ad033e6d73e14730ac46511c96aaf826
Source noteuspto-grants-2014_08