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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451742Generated: October 31, 2026

Water → HCID 59382849, compound

https://huagongshe.com/reaction/451742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 59382970HCID 59382970—
SolventDichloromethaneHCID 6344—
ProductHCID 59382849HCID 5938284980.5%

Reaction Steps

To a mixture solution of tert-butyl (S)-1-(4-(t-butyldimethylsilyloxy)cyclohexyl)-3-(methylamino)propan-2-ylcarbamate (112 g, 209 mmol) and Et3N (52.8 g, 522 mmol) in CH2Cl2 (1200 mL) was added dropwise a solution of benzyl chloroformate (39 g, 230 mmol) in CH2Cl2 (40 mL) at −20° C. After stirring for an additional 2 h, water (400 mL) was added and the mixture was extracted with CH2Cl2 (2×200 mL). The organic layers were washed with brine, dried over MgSO4, and evaporated. The residue was purified by silica chromatography to afford crude tert-butyl (S)-1-(4-(t-butyldimethylsilyloxy)cyclohexyl)-3-(N-(benzyloxycarbonyl)-N-methylamino)propan-2-ylcarbamate (90 g) as an oil which was a mixture of two isomers. The isomers were separated by preparative HPLC. 1H NMR (CDCl3, 400 MHz): δ=0.08 (s, 6H), 0.89 (s, 9H), 1.28 (m, 4H), 1.40 (d, 9H), 1.59 (m, 4H), 2.96 (d, 3H), 3.05 (d, 1H), 3.15 (d, 1H), 3.45 (t, 3H), 3.90 (s, 1H), 5.12 (d, 2H), 7.33 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-04b4275c61eb457a8486b39ef817a9eb
Source noteuspto-grants-2013_07