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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118237Generated: October 30, 2026

Triethylamine → HCID 178455455, compound

https://huagongshe.com/reaction/2118237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178455454HCID 178455454—
SolventDichloromethaneHCID 6344—
ProductHCID 178455455HCID 178455455106.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

To an ice-cooled solution of 27.6 g (107 mmol) of trans-[4-(tert-butyl-dimethyl-silanyloxymethyl)-cyclohexyl]-methanol and 9.99 mL (128 mmol, 1.2 eq) of methanesulfonyl chloride in 350 mL of CH2Cl2 were added under stirring at 0-10° C. 29.6 mL (213 mmol, 2 eq) of Et3N within 20 min. The reaction mixture was then stirred at RT for 1 h. It was then partitioned between CH2Cl2, 1M HCl and water. The CH2Cl2-phase was dried over MgSO4 and concentrated to yield 38.2 g of crude trans-methanesulfonic acid 4-(tert-butyl-dimethyl-silanyloxymethyl)-cyclohexylmethyl ester as colorless viscous oil, MS: 354 (M+NH4+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442791B2
Source datasetuspto-grants-2008_10
ORD IDord-c221c22bc1304c25a6ab1f0b13a03ed1
Source noteuspto-grants-2008_10