Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698753Generated: October 26, 2026

Water → 135367-08-7

https://huagongshe.com/reaction/1698753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosuccinimideHCID 31398—
ReactantPotassium BromideHCID 253877—
Reactant2beta-Carbomethoxy-3beta-(4-trimethylsilylphenyl)tropaneHCID 69736376—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
Product135367-08-7HCID 57340111100.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2β-Carbomethoxy-3β-(4′-trimethylsilylphenyl)tropane (594 mg, 1.79 mmol) and KBr (320 mg, 2.68 mmol) in 15 mL of acetic acid and 2 mL of MeOH was stirred at 60° C. for 20 min. 285 mg of NCS (2.15 mmol) was added at one time and the resulting mixture was stirred at the same temperature for 4 hrs. After cooling to rt 100 mL of H2O and 50 mL of Et2O were added. The aqueous phase was separated and the organic phase was extracted with 3N HCl (20 mL). The combined aqueous phase was washed with 20 mL of Et2O, basified with concentrated NH4OH and extracted with CH2Cl2 (2×50 mL). The solution was then dried and the removal of the solvent in vacuo gave the pure product as a white solid (607 mg, 100%). m.p. 114-116° C. 1H NMR (CDCl3, 400 MHz) δ 7.38 (d, J=8.4 Hz, 2H), 7.13 (d, J=8.4 Hz, 1H), 3.58-3.55 (m, 1H), 3.51 (s, 3H), 3.38-3.36 (m, 1H), 2.98-2.86 (m, 2H), 2.56 (dt, J−12.8, 2.8 Hz, 1H), 2.23 (s, 3H), 2.26.2.05 (m, 2H), 1.75-1.58 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344179B1
Source datasetuspto-grants-2002_02
ORD IDord-a43917e772484797aa478e2e62be5eda
Source noteuspto-grants-2002_02