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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866692Generated: November 1, 2026

Hydrochloric Acid → HCID 86616401, compound

https://huagongshe.com/reaction/1866692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86616400HCID 86616400—
SolventDichloromethaneHCID 6344—
ProductHCID 86616401HCID 86616401—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a stirred solution of oxalyl chloride (0.91 mL, 10.4 mmol) in CH2Cl2 (40 mL) at −78° C. was added DMSO (1.48 mL, 20.9 mmol), dropwise, over 5 min. The reaction mixture was stirred for 30 min, during which time it warmed to −60° C., then a solution of tert-butyl [4,6-difluoro-1-(hydroxymethyl)-2,3-dihydro-1H-inden-1-yl]carbamate from Step E (2.08 g, 6.95 mmol) in CH2Cl2 (22 mL) was added, dropwise, over 30 min. During the addition, the reaction temperature rose to −45° C. and it was stirred at this temperature for an additional 15 min. To the resulting mixture was added N,N-diisopropylethylamine (7.28 mL, 41.7 mmol), dropwise, over 2 min. The mixture was allowed to warm to 0° C., stirred for 15 min then poured into ice (60 mL) and 1 N aqueous HCl (30 mL). The resulting mixture was extracted with CH2Cl2 (2×100 mL). The combined organic extracts were washed with H2O (30 mL), then brine (50 mL), then dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound. MS: m/z=224 (M−OC4H9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629338B2
Source datasetuspto-grants-2009_12
ORD IDord-bc7031227f6c435899627b7905f25ac7
Source noteuspto-grants-2009_12